Congenital Disorders
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Down Syndrome | Genetic, has 47 chromosomes instead of the usual 46, mild to severe retardation with characteristic facial features and distinctive physical abnormalities
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Down Syndrome Symptoms: | Sm head, with a flat back skull
Slant to the eyes; flat nasal bridge
Sm low-set ears
Sm mouth with a protruding tongue
Sm weak muscles
Short hands w/stubby fingers; deep horiz. crease across the palm
Exaggerated space btwn the big and little toes
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Down Syndrome Diagnosis and Prevention: | Prenatally via ultrasound, blood tests and/or amniocentesis or during the neonatal period; no prevention
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Down Syndrome Etiology: | Have extra chromosome number 21 (trisomy 21). Occurs in 1 to 650 births and more to woman over age 35.
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Down Syndrome Treatment: | No known cure; treatment plan is individual and includes a multidimensional approach to maximize the development of motor and mental skills.
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Cerebral Palsy (CP) | most common crippler of children; congenital or acquired, bilateral or unilateral paralysis from damage to CNS
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Cerebral Palsy Symptoms and Signs: | Infant has difficulty with sucking and swallowing
Muscles may be floppy or stiff
When infant is lifted from behind, the legs may be difficult to separate and they may cross their legs
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Spastic CP | Hyperactive reflexes or rapid muscle contractions
Scissor gait by walking on the toes and crossing one foot over the other
70% of cases
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Athetoid CP | Involuntary muscle movements, especially during stress Reduced muscle tone
Difficulty with speech
20 % of cases
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Ataxic CP | Lack of control over voluntary movements
Poor balance and wide gait
Visual and auditory deficits
Seizure activity
Mental retardation
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Cerebral Palsy Patient Screening: | Suspected during routine well-baby or well-child visits
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Cerebral Palsy Etiology: | Stems from inadequate blood or oxygen supply to the brain during fetal development, during the birth process or in early childhood until about 9 years of age.
More common in premature infants and in male babies.
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Cerebral Palsy Diagnosis and Prevention: | Made from a clinical picture and neurologic examination findings.
Prevention in head injury or brain infection in prenatal, perinatal and neonatal periods.
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Cerebral Palsy Treatment: | No cure; goal of treatment is to minimize the handicap by providing every possible therapeutic measure to help the child reach their potential.
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Cerebral Palsy Prognosis: | Brain damage can't be reversed; therefore there is no cure for CP.
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Spina Bifida | Group of malformations of the spine in which the posterior portion of the bony canal containing the spinal cord is completely or partially absent.
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Spina Bifida Occulta | The posterior arches of the vertebrae, commonly in the lumbosacral area, fail to fuse, but there is no herniation of meninges or spinal cord. Usually there is no spinal cord or spinal nerve involvement.
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Spina Bifida Symptoms and Signs: | Without displacement of the cord or the meninges it is asymptomatic.
Evidence of neural tube defect dimpling, a tuft of hair or hemangioma over the site where the vertebrae have not completely fused.
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Spina Bifida Patient Screening: | Discovered during the newborn examination.
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Spina Bifida Etiology: | Congenital anomaly is unknown, but it has been associated with exposure t ionizing radiation during the early uterine life.
Reduced levels of Vitamin A and folic acid during pregnancy may contribute.
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Spina Bifida Diagnosis and Prevention: | Maternal blood levels of AFP measured
Ultrasound
Postnatal physical examination
Prevention is unknown; avoiding exposure to ionizing radiation is wise
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Spina Bifida Treatment: | Surgery to repair the defect if the child becomes symptomatic with neurologic problems
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Spina Bifida Prognosis: | Prognosis is good.
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Hydrocephalus | Abnormal enlargement of the head due to the amount of CSF increased and it's circulation is blocked. "Water on the brain"
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Hydrocephalus Symptoms and Signs: | Fontanelles befin to bulge
Sutures of the skull separate
Scalp veins become distended
Head circumference increases
Infant has a high pitched cry, is irritable and projectile vomit
Downward displacement of the eyes
Abnormal muscle tone of the legs
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Hydrocephalus Patient Screening: | Detected during newborn examination by measuring the head circumference and plotting on a growth chart
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Hydrocephalus Etiology: | A large amount of CSF accumulates in the skull, causing increased intracranial pressure. It may be caused by a lesion within the system or by a congenital structural defect. Intracranial hemorrhage
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Hydrocephalus Diagnosis and Prevention: | Made through clinical picture, physical examination, and radiographic skull studies.
MRI and CT
No known prevention for congenital form; good prenatal care, preventing infections and injury to head during childhood
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Hydrocephalus Treatment: | Placing a shunt in the ventricular or subarachnoid spaces to drain off the excessice CSF
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Hydrocephalus Prognosis: | Varies depending on the extent; most children can function normally in society
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Congenital Cardiac Defects | Developmental anomalies of the heart or the great vessels of the heart and present at birth
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Acyanotic Defects | Oxygenated blood does not mix with deoxygenated blood and the infant usually maintains a fairly normal pink skin color. Cyanosis is not prevalent.
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Ventricular Septal Defect | Most common congenital cardiac disorder, ventricular septal defect (VSD), it's an abnormal opening btwn the RT and LT ventricles.
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Patent Ductus Arteriosus (PDA) | Results when the ductus fails to functionally close.
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Coarctation of the Aorta | Characterized by a narrowed aortic lumen, causing a partial obstruction of the flow of blood through the aorta.
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Atrial Septal Defect (ASD) | An abnormal opening between the right and left atria.
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Tetralogy of Fallot | Most common cyanotic cardiac defect, it's a combo of 4 congenital heart defects: VSD, pulmonary stenosis, dextroposition of the aorta and right ventricular hypertrophy
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Transposition of the Great Arteries | The aorta and the pulmonary artery are reversed, resulting in two closed-loop circulatory systems.
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Cleft Lip (harelip) | Congenital birth defect consisting of one or more clefts in the upper lip.
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Cleft Palate | A birth defect in which there is a hole in the middle of the roof of the mouth (palate).
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Cleft Lip and Palate Etilogy and Prevention: | The failure in embryonic development of the fetus. 1 in 10,000 births. No prevention for this deformity.
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Congenital Pyloric Stenosis | A gastric obstruction associated with narrowing of the pyloric sphincter at the exit of the stomach.
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Congenital Pyloric Stenosis Symptoms: | Infant has episodes of projectile vomiting, after feedings and gails to gain weight. Symptoms usually begin at 2 to 3 weeks of age.
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Congenital Pyloric Stenosis Etiology and Diagnosis: | Slight hereditary tendency, but exact cause is unknown. Diagnosed from the history and pt's physical condition, upper GI x-ray and ultrasound of the pylorus.
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Congenital Pyloric Stenosis Treatment and Prevention: | Surgical intervention in which the constricted pylorus is incised and sutured to relieve the obstruction. No prevention known.
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Cystic Fibrosis | An autosomal recessive inherited disorder, is a chronic dysfunction the gene called cystic fibrosis transmembrane conductance regulator (CFTR) that affects multiple systems. Most common fatal genetic disease.
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Cystic Fibrosis Symptoms and Signs: | Attacks the lungs and digestive system, producing thick and sticky mucus that accumulates and blocks glandular ducts. Sinus infections and diarrhea.
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Cystic Fibrosis Etiology and Diagnosis: | Inherited and transmitted as an autosomal recessive trait. Genetic testing and sweat test.
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Cystic Fibrosis Treatment and Prognosis: | Considered fatal and treatment is supportive measures to help lead a normal life and prevent pulmonary infections.
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Bronchopulmonary Dyplasia (BPD) | serious, chronic lung disease, results after and insult to the neonate's lungs; may be sequela to IRDA, lung infection or extreme prematurity; lungs are hard, stiff and hard to ventilate
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BPD Symptoms and Signs: | Periods of dyspnea
Tachypnea
Wheezing
Cyanosis
Nasal Flaring
Sternal Refractions
O2 saturation and heart rate decreases
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Infant Respiratory Distress Syndrome (IRDS) | patient suffers acute hypoxemia caused by infiltrates within the alveoli
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BPD Diagnosis and Treatment: | Observation
Chest X-ray
Oxygen and CO2 levels tested
Atrial blood gases tested
Replacement of the damaged alveoli
Supplemental O2 therapy
Diuretics and Antiinflammatory drugs
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Laryngomalacia | obstructive airway condition; infant exhibits respiratory stridor that is louder on inspiration
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Tracheomalacia | obstructive airway condition; infant exhibits respiratory stridor that is louder on expiration
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Bronchomalacia | means 'floppiness' of some part of the bronchi. Patients present with noisy breathing and/or wheezing. There is collapse of a main stem bronchus on exhalation.
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Laryngo, Tracheo and Bronchomalacia Diagnosis: | Chest X-Ray
CT
Laryngoscopy
Bronchoscopy
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Retinopathy of Prematurity | or Retrolental Fibroplasia; is an abnormal growth of the blood vessels in the retinas of the infant's eyes
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Retinopathy Symptoms and Signs: | occurs most often in infant's before 28 weeks, no visible symptoms
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Retinopathy Diagnosis and Treatment: | Diagnosed by ophthalmologist using a ophthalmoscope
Most mild forms resolve without treatment
Laser treatment
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Necrotizing Entercolitis (NEC) | is an acute inflammatory process cuased by ischemic necrosis of the mucosal lining of the small intestine, large intestine or both
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NEC Symptoms and Signs: | Feeding intolerance
Abdominal distention
Bile-colored emesis
Diarrhea
Blood in Stool
Lethargy
Decreased or absent bowel sounds
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NEC Diagnosis and Treatment: | Etiology is inknown
Observation of feeding patterns or activity level
Respiratory difficulties
Abdominal distention and tenderness
CBC and stool cultures
Feedings stopped and feeding tube placed
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Croup | is an acute, severe inflammation and obstruction of the respiratory tract
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Croup Symptoms and Signs: | Hoarseness
Fever
Harsh, high-pitched cough
Stridor during inspiration
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Croup Diagnosis and Treatment: | Blood and Throat Cultures
Laryngoscopy
X-Rays of airway
Treated symptomatically, steroids, increased fluid intake, antibiotics
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Adenoid Hyperplasia | is an abnormal enlargement of the lymphoid tissue located in the space above the soft palate of the mouth, causing a partial breathing blockage
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Adenoid Hyperplasia Symptoms, Diagnosis and Treatment | Mouth-breathing and snoring
Lateral pharyngeal x-ray and nasopharyngoscopic exam
Adenoidectomy
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Asthma | a chronic reversible obstructive disease caused by increased reactivity of the tracheobronchial tree to stimuli
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Asthma Symptoms and Signs: | Productive or nonproductive cough
Wheezing
Rapid pulse
Pallor
Profuse perspiration
"Tight chest"
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Asthma Diagnosis: | Pulmonary function test
X-ray
Intradermal skin test to identify inhalant and food allergies
Blood test (CBC with differential leukocyte count
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Asthma Treatment: | Medical management
Immunotherapy
Allergy shots
Steroid injections
Inhalation therapy
Hospitalization
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Bronchiolitis | an inflammation of the bronchioles, the smallest air passages of the lungs, which is usually caused by viruses, such as RSV
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Bronchiolitis Symptoms and Signs: | Cough and nasal congestion
Wheeze
Tachypnea
Respiratory distress
Apnea
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Bronchiolitis Diagnosis: | Pt History
Physical examination
Chest X-ray
Rapid RSV testing
Viral culture from the nasopharynx
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Bronchiolitis Treatment: | Supportive care
Nebulizer treatment
Supplemental oxygen
IV fluids, if necessary
Intubation/Ventilator until the infection runs course
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Neuroblastoma | a cancer of the sympathetic nervous system, it's the 3rd most common childhood malignancy; arises from primitive sympathetic ganglion cells
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Neuroblastoma Symptoms ans Signs: | Abdominal mass
Abdominal pain or fullness
Anemia
Bone pain
Fever
Hypertension
Weight loss
"Raccoon Eyes"
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Neuroblastoma Diagnosis: | Measurement of urine serum catecholamine levels
Electrolytes, kidney and liver function
Biopsy of the mass
Chest X-ray
Chest and head CT
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Neuroblastoma Treatment: | Surgical removal
Chemotherapy
Autologous hematopoietic stem cell rescue
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Chickenpox | a highly contagious, acute viral infection; systemic disease with superficial cutaneous lesions
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Chickenpox Symptoms and Sign: | Lesions that progress to papules then to vesicles that form crusts
May experience fever, malaise and anorexia
Possible bacterial infection, viral pneumonia, conjunctival ulcers and Reye syndrome
Itchy
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Chickenpox Diagnosis and Treatment: | History of exposure and the presence of characteristic cutaneous eruptions
Soda baths
Calamine lotion
Acetaminophen for fever and pain
Antiviral drugs
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Developmental Dysplasia of the Hip | an abnormal development of the hip joint that ranges from an unstable joint to dislocation of the femoral head from the acetabulum
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Developmental Dysplasia of the Hip Symptoms: | Asymmetric folds of the thigh
Shortening of the femur when the knees and hips are flexed at right angles
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Developmental Dysplasia of the Hip Diagnosis: | Abnormal signs, including positive Ortolani and Barlow maneuvers, may be detected at birth.
Physical examination and ultrasound
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Developmental Dysplasiaof the Hip Treatment: | After femur head is returned to its proper position in the acetabulum, the legs are held in place by a Pavlik harness, a splint, or a cast
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Hypertrophic Cardiomyopathy | a congenital disorder, occurs when a portion of the heart muscle thickens without any apparent cause; major cause of sudden cardiac death in young athletes who have appeared to be completely healthy
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Hypertrophic Cardiomyopathy Symptoms and Signs: | First sign is collapse of a seemingly healthy young athlete
Chest pain
Syncope
Hypertension
Palpitations
SOB
Fatigue
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Hypertrophic Cardiomyopathy Diagnosis: | Autopsy
Drop in blood pressure
Family history
Holter monitor
Electrocardiogram (ECG)
X-ray
MRI
Genetic test
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Hypertrophic Cardiomyopathy Treatment: | Beta-Blockers
Calcium Channel Blockers
Pacemaker
Implantable Cardioverter-Defribillator (ICD)
Surgical myectomy
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Common Variable Immunodeficiency (CVID) | an acquired B-cell deficiency that results in decreased antibody production and/or function
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CVID Symptoms and Signs: | History of chronic or recurrent infections, such as pneumonia, bronchitis, sinusitis, otitis media
Gastrointestinal (GI) disease
Lymphadenopathy, splenomegaly and hepatomegaly
Chronic lung disease and granulomatous disease
Autoimmune disorders
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CVID Etiology and Diagnosis: | has 2 peaks of incidence: 1 btwn ages 18 to 25 and smaller peak btwn 1 to 5 years
History of repeated and chronic infections lead to investigation of immunoglobulin levels and T-cell quantities
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Common Variable Immunodeficiency (CVID) Treatment: | aimed at preventing infections and implementing early treatment with appropriate antibiotic administration when infections occur
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Severe Combined Immunodeficiency (SCID) | is a group of disorders that result from a disturbance in the development and function of the T cells with or without B cells
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Severe Combined Immunodeficiency (SCID) Symptoms: | Severe, recurrent infrections with bacteria, viruses, fungi and protozoa; chronic diarrhea; and failure to thrive
Occurs by the age of 3 to 6 months
Common infections: Pneumocystis Pneumonia and Persistent Mucocutaneous Candidiasis
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SCID Etiology and Diagnosis: | 2 types: X-linked and autosomal recessive; both lead to defects in stem cell differentiation into B cells and T cells
Routine newborn screen
Immunoglobulin levels measured
Antibody titers measured
#'s of T cells and B cells measured
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Severe Combined Immunodeficiency (SCID)Treatment: | Bone marrow transplant (BMT)
Gene therapy
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Pernicious Anemia | is caused by chronic atrophic gastritis resulting in decreased gastric production of hydrochloric acid and a shortage of intrinsic factor
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Pernicious Anemia Symptoms: | Sore tongue
Weakness
Tingling and numbness in the extremities
Lips, tongue and gums appear pale whereas the sclera and skin appear slightly jaundiced
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Pernicious Anemia Etiology and Diagnosis: | 90% of pts have anti-parietal antibodies, which can be cytotoxic to the parietal cells
Lab and blood tests
Schilling test
Bone marrow test
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Pernicious Anemia Treatment: | Injection of Vitamin B12 for life
Blood replacement
Supportive measures
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Idiopathic Thrombocytopenic Purpura (ITP) | is a acquired disorder that results from an isolated deficiency of platelets
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ITP Symptoms : | Inability of blood to clot
Spontaneous hemorrhages in the skin, mucous membranes or internal organs
Petechiae
Ecchymoses
Nosebleeds
GI bleeding
Menorrhagia
Hematuria
Easy bruising
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ITP Etiology and Diagnosis: | Considered idiopathic (of unknown cause)
Causes of thrombocytopenia ruled out first
Complete CBC analysis and peripheral blood smear
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Idiopathic Thrombocytopenic Purpura (ITP) Treatment: | Corticosteroid administration
IVIG may be administered to increase platelet count
Anemia needs to be corrected with blood transfusion
Vitamin K administration
Splenectomy last resort
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Systemic Lupus Erythematosus (SLE) | is a chronic, inflammatory autoimmune disease characterized by unusual autoantibodies in the blood that target tissues of the body
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SLE Symptoms and Signs: | inflammation of the skin, joints, nervous system, kidneys, lungs and other organs.
Butterfly rash or erythema
Photosensitivity
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Systemic Lupus Erythematosus (SLE) Diagnosis: | Blood and urine tests
Chest x-ray and echocardiogram
Biopsy of kidney tissue
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Systemic Lupus Erythematosus (SLE) Treatment: | Anti-inflammatory drugs
Corticosteroids
Immunosuppressive agents
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Scleroderma | a chronic, progressive disease characterized mostly by sclerosis of the skin, scarring of certain internal organs
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Scleroderma Symptoms and Signs: | Characterized by sclerosis and shrinking of the skin and certain internal organs (GI tract, heart, lungs and kidneys)
Skin becomes taut, firm and edematous
Skin feels tough and leathery, may itch
Pigmented patches
Swelling, stiffness, joint pain
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Scleroderma Etiology and Diagnosis: | Cause is unknown, appears to be autoimmune disease
Complete history and physical exam
Lab testing including Scl-70 and centromere antibodies
Blood tests and urinalysis
CAT of the chest and right heart catheterization
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Scleroderma Treatment: | No specific treatment
Treatment is directed to area of body affected
Physical therapy for muscle strength
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Sjogren Syndrome | is an autoimmune disease that features inflammation in moisture-secreting glands; resulting in dryness in the affected areas
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Sjogren Syndrome Etiology and Diagnosis: | Genetic factors seem to play a role; most are female
Screened for medication side effects, autoimmune thyroid disease, RA, SLE, sarcoidosis and scleroderma
Schirmer testing for dry eyes
Lower lip biopsy to check lymphocytes
Blood test
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Sjogren Syndrome Treatment: | Is directed toward relieving symptoms
Increasing fluid intake, chewing gum, oral sprays
Prednisone and/or antimalarial medications
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Rheumatoid Arthritis (RA) | is a chronic, inflammatory, systemic disease that affects the joints
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RA Symptoms and Signs: | Inflammation and edema of the synovial membranes surrounding a joint
Joint deformity
Pain
Joint stiffness
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RA Diagnosis: | Is based on a review of the symptoms, pt and FH, physical exam, x-rays and blood tests that check elevated levels of rheumatoid factor
CBC
Synovial fluid analysis
Serum protein electrophoresis
ESR
Citrulline antibody
Antinuclear antibody titer
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RA Treatment: | Reduction in inflammation and pain
Preservation of joint function
Prevention of joint prevention
Anti-inflammatory medications
Corticosteroids
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Multiple Sclerosis (MS) | is an inflammatory disease of the central nervous system; attacks the myelin sheath, causing scarring that debilitates the nerves
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MS Symptoms and Signs: | Weakness or numbness in 1 or more limbs
Optic neuritis
Loss of vision in one eye
Diplopia
Unsteady gait
Vertigo
Difficulty with urinating, leading to UTIs
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MS Diagnosis: | Challenging to diagnose
Physical exam in early stages
MRI
Determined by eliminating other possible causes
Exam of CSF
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MS Treatment: | Acute attacks are treated with corticosteroids
Immunosuppressive therapies
Biologic medications
Treated systemically
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Myasthenia Gravis | is a chronic, progressive neuromuscular disease that is caused by autoantibodies to the acetylcholine receptor at nerve synapses
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Myasthenia Gravis Symptoms and Signs: | Extreme muscular weakness (without atrophy)
Progressive fatigue
Drooping eyelids
Diplopia
Difficulty with talking , chewing and swallowing
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Myasthenia Gravis Diagnosis: | Physical examination is done that aims to test for fatigability of different muscle groups
Tensilon test
EMG
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Myasthenia Gravis Treatment: | Treatment is symptomatic and supportive
Anticholinesterase drugs
Mestinon
Corticosteroids
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Cushing Syndrome | is a condition of chronic hypersecretion of the adrenal cortex, which results in excessive circulating cortisol levels
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Cushing Syndrome Symptoms and Signs: | Fatigue
Muscular weakness
Weight Gain
Changes in body appearance
Moon Face
Thin skin, bruise easy
Stretch marks
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Cushing Syndrome Diagnosis: | Physical appearance: moon face, buffalo hump and gross obesity of the trunk
Urinalysis
CT or MRI
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Cushing Syndrome Treatment: | Treatment depends on cause of the over secretion of cortisol; if tumor is cause, surgical removal or radiation of the tumor in the pituitary gland or adrenal gland
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Hypoparathyroidism | is the condition in which the secretion of parathyroid hormone (PTH) by the parathyroid glands is greatly reduced
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Hypoparathyroidism Symptoms: | Hypocalcemia
Numbness and tingling of fingertips, toes, ears or nose followed by muscular spasms or twitching of the hands and feet
Tetany
Emotional changes, irritability, confusion
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Hypoparathyroidism Diagnosis: | Blood studies
ECG
Clinical picture of neuromuscular hyperexcitability
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Hypoparathyroidism Treatment: | Calcium replacement therapy with vitamin D for life
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Hyperparathyroidism | is a condition caused by overactivity of 1 or more of the 4 parathyroid glands and results in the overproduction of PTH
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Hyperparathyroidism Symptoms: | Muscle weakness
Atrophy
GI pain
Nausea
Low back pain
Renal calculi
Bone tenderness
Arthritis type of pain
Easy fracturing of bones
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Hyperparathyroidism Treatment: | Varies with the cause and is highly individualized
Parathyroid surgery
Reduce blood serum calcium levels by medication
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Hyperparathyroidism Diagnosis: | X-ray
Bone density test
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Hypothyroidism | a very common condition, refers to state in which thyroid hormone production is below normal
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Hypothyroidism Symptoms: | Fatigue
Cold intolerance
Constipation
Dry, flaky skin
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Hypopituitarism | is a condition caused by a deficiency or absence of any of the pituitary hormones, produced by the anterior pituitary lobe
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Hypopituitarism Symptoms: | Stomach pain, decreased appetite, nausea, vomiting, constipation
Excessive thirst and urination
Fatigue and/or weakness
Anemia
Headache and dizziness
Sensitivity to cold
Weight loss or weight gain
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Hypopituitarism Diagnosis: | Medical evaluation to detect partial or selective hormone deficiencies
Contributors are history of head trauma, previous radiation or surgical procedure to the gland or nearby tissue
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Hypopituitarism Treatment: | Age, severity and type of deficiency and underlying cause determine the source of treatment
Replacement therapy with hormonal supplements
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Diabetes Insipidus | is a disturbance of water metabolism resulting in extreme thirst and excessive secretion of dilute urine
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Diabetes Insipidus Symptoms: | Extreme thirst
Excretion of an excessive amount of diluted urine
Unexplained fussiness or inconsolable crying
Trouble sleeping
Fever
Vomiting
Diarrhea
Delayed growth
Weight loss
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Diabetes Insipidus Diagnosis: | Water deprivation test
Urinalysis
Magnetic resonance imaging (MRI)
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Diabetes Insipidus Treatment: | Vasopressin injections
Nasal spray
Oral desmopressin acetate (DDAVP)
Thiazide diuretics
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Goiter | refers to any enlargement of the thyroid gland usually evidenced by a swelling in the neck
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Goiter Symptoms: | Asymptomatic in early stages
Usually female
Difficulty swallowing
Dyspnea
Weight loss
Heat intolerance
Tachycardia
Anxiety
Increased sweating
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Goiter Etiology and Diagnosis: | Results from a shortage of iodine in diet
Exam of neck
Blood studies indicate thyrotropin levels
Measurement of radioactive iodine uptake by the thyroid gland
Thyroid ultrasonography
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Goiter Treatment: | A drop per week of saturated solution of potassium iodide
Adding iodine to diet
Avoidance of goitrogenic drugs or food
Thyroid hormone T4
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Graves Disease | a condition of primary hyperthyroidism, occurs when the entire thyroid gland hypertrophies, resulting in a diffuse goiter and an overproduction of thyroid hormones
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Graves Disease Symptoms: | Increased metabolism and multisystem changes
Rapid heartbeat and palpitations
Nervousness
Excitability
Insomnia
Excessive appetite, but loses weight
Profuse perspiratio
Muscular weakness
Tremor
Loss of hair
Outward protrusion of eyes
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Graves Disease Diagnosis: | Clinical picture and history
Serum T3,and T4 levels are tested
Thyroid scan
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Graves Disease Treatment: | Reduce the formation and secretion of thyroid hormone
Antithyroid drugs
Radioactive iodine therapy
Thyroidectomy
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Hypoglycemia | is an abnormally low glucose level of the blood
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Hypoglycemia Symptoms: | Sweating
Nervousness
Weakness
Hunger
Dizziness
Trembling
Headache
Palpitations
Confusion
Visual disturbances
Stupor
Coma
Drunkenness behavior
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Hypoglycemia Diagnosis: | Physical exam
Check blood glucose level
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Hypoglycemia Treatment: | Intravenous infusion of glucose
Hormone glucagon given
A complex carbohydrate and protein snack
Modified diet
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Hashimoto Thyroiditis | Aka Chronic Lymphocytic Thyroiditis
A chronic disease of the immune system that attacks the thyroid gland
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Hashimoto Thyroiditis Symptoms: | Gradual and and painless lumpy enlargement of the thyroid gland
Pressure in the neck
Difficulty swallowing
Sensitivity to cold
Weight gain
Fatigue
Depression
Mental apathy
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Hashimoto Thyroiditis Diagnosis: | Thyroid gland needle biopsy
Radioactive iodine uptake scan
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Hashimoto Thyroiditis Treatment: | Lifelong replacement of thyroid hormones
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Diabetes Mellitus (DM) | is a chronic disorder of carbohydrate, fat and protein metabolism caused by inadequate production of insulin by the pancreas or faulty use of insulin by the cells
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DM Symptoms and Signs: | Increased thirst
Frequent urination
Extreme hunger
Unexplained weight loss
Presence of ketones in the urine
Fatigue
Irritability
Blurred vision
Slow-healing sores
Frequent infections, such as gums or skin infections and vaginal infections
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DM Diagnosis: | Patient History
Assessment for cardinal symptoms
At least 2 positive tests of fasting blood plasma glucose, presence of glucose and acetone in the urine
Blood insulin test
Eye exam for retinopathy
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DM Treatment: | Normalize blood glucose
Well-balanced diet
Insulin administration
Oral medication
Exercise
Blood and urine testing
Hygienic measures
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Gestational Diabetes | is a condition of damaged ability to process carbohydrate that has its onset during pregnancy
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Gestational Diabetes Symptoms: | Polyuria
Polydipsia
Polyphagia
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Gestational Diabetes Diagnosis: | Routine prenatal urine glucose test
Fasting blood glucose determination
Glucose tolerance tests
Glycated hemoglobin tests
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Gestational Diabetes Treatment: | Eat balanced meals
Exercise
Check blood sugar levels
Monitor fetal growth and well-being
Take diabetes medication and insulin shots
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