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QuestionAnswer
Physiologic Jaundice H: Onset after 24 hours of life.
Breast Milk Jaundice H: Jaundice onset after 3-5 days, continuing into weeks/months.
ABO Incompatibility (Hemolysis) H: Onset within the first 24 hours of life.
Gilbert's Syndrome (for older children) H: Intermittent jaundice, often with fasting or stress/illness.
Familial Short Stature H: Short stature in parents/family members.
Constitutional Growth Delay H: History of a family member being a "late bloomer" (delayed puberty).
Growth Hormone Deficiency H: Deceleration of growth rate (crossing centiles) over time.
Chronic Systemic Disease H: History of an underlying chronic illness (e.g., bloody stools in IBD).
Constitutional Delay of Puberty H: Delayed puberty in a parent ("late bloomer" family history).
Central Precocious Puberty H: Onset of secondary sex characteristics <8 in girls / <9 in boys.
Hypogonadotropic Hypogonadism H: Puberty absent by late teens; often associated with anosmia (Kallmann).
Primary Hypothyroidism H: Early signs of slow growth, lethargy, or constipation.
Iron Deficiency H: Excessive cow's milk intake or prolonged vegetarian/vegan diet.
Vitamin D Deficiency H: Limited sun exposure or exclusively breastfed without supplementation.
Fibre Deficiency H: Diet low in fruits, vegetables, and whole grains; frequent fast food.
Folate Deficiency H: History of chronic poor intake or use of certain medications (e.g., methotrexate).
Measles H: History of prodromal fever/cough/coryza/conjunctivitis.
Mumps H: History of fever and pain when chewing.
Rubella H: History of a mild, non-specific prodrome.
Varicella (Chickenpox) H: Exposure history 10-21 days prior; rash started on the trunk.
Hypovolemic Shock H: History of significant fluid loss (vomiting, diarrhea, hemorrhage).
Septic Shock H: History of preceding infection (e.g., pneumonia, cellulitis, UTI).
Cardiogenic Shock H: History of known heart disease or acute event (e.g., myocarditis).
Anaphylactic Shock H: Recent exposure to a known or new allergen (food, sting, medication).
Ventricular Septal Defect (VSD) H: Symptoms of heart failure (poor feeding, diaphoresis) if large.
Atrial Septal Defect (ASD) H: Often asymptomatic until later childhood or adulthood.
Patent Ductus Arteriosus (PDA) H: Often symptomatic in preemies; history of recurrent lung infections.
Tetralogy of Fallot (TOF) H: History of cyanotic spells (Tet Spells); squatting behavior in older children.
Allergic (Extrinsic) Asthma H: Symptoms triggered by specific allergens (dust, pollen, pets).
Viral-induced Asthma H: Wheezing episodes occur exclusively during/after a cold or viral illness.
Exercise-induced Bronchoconstriction H: Symptoms occur 5-15 minutes into strenuous physical activity.
Cough-variant Asthma H: Chronic, persistent, non-productive cough (especially at night).
Congenital Hypothyroidism H: Neonatal lethargy, poor feeding, or prolonged jaundice.
Acquired Primary Hypothyroidism H: Gradual onset of fatigue, cold intolerance, constipation.
Hyperthyroidism (Graves' Disease) H: Unexplained weight loss with increased appetite; nervousness.
Thyroid Nodules H: Sensation of a lump in the neck or hoarseness.
Congenital Adrenal Hyperplasia (CAH) H: History of salt-wasting crisis (vomiting, dehydration) in a neonate.
Addison's Disease (Primary Adrenal Insufficiency) H: Gradual onset of fatigue, weakness, salt craving.
Cushing's Syndrome H: Slow growth despite weight gain.
Adrenal Tumors (e.g., Pheochromocytoma) H: Paroxysmal (episodic) symptoms of headache, palpitations, sweating.
Infections (e.g., Tuberculosis, Abscesses) H: History of exposure (TB) or persistent, localized symptoms after an illness.
Connective Tissue/Inflammatory Diseases H: Fever pattern (e.g., quotidian fever in Systemic JIA) with joint symptoms.
Neoplastic Diseases (e.g., Leukemia, Lymphoma) H: Unexplained night sweats, easy bruising, bone pain.
Miscellaneous Causes (e.g., Drug fever) H: Recent new medication or drug exposure history.
Roseola Infantum (HHV-6) H: High fever (3-5 days) that resolves before the rash appears.
Erythema Infectiosum (Fifth Disease - Parvovirus B19) H: History of preceding mild, non-specific cold symptoms.
Hand-Foot-and-Mouth Disease (Coxsackievirus) H: History of painful oral intake; exposure at daycare.
Varicella (Chickenpox) H: Rash started on the trunk; appears in "crops."
Acute Gastroenteritis H: Acute onset of vomiting and non-bloody diarrhea.
Constipation H: Painful defecation and stool withholding behavior.
Gastroesophageal Reflux Disease (GERD) H: Frequent post-prandial vomiting (spitting up); irritability after feeds.
Functional Abdominal Pain/IBS H: Chronic, recurrent abdominal pain not associated with alarming symptoms.
Childhood Absence Epilepsy H: Brief, frequent episodes of staring/blanking out with sudden onset/offset.
Benign Epilepsy with Centrotemporal Spikes (Rolandic Epilepsy) H: Seizures occur primarily at night/upon waking; face/mouth jerking.
Juvenile Myoclonic Epilepsy (JME) H: History of brief, involuntary muscle jerks (myoclonus) upon waking.
Infantile Spasms (West Syndrome) H: Clusters of sudden, brief flexor/extensor spasms in an infant.
Celiac Disease H: Symptoms begin after the introduction of gluten (wheat, barley, rye).
Cystic Fibrosis (Pancreatic insufficiency) H: History of recurrent respiratory infections and very foul-smelling, fatty stools (steatorrhea).
Chronic Diarrhea/Gastroenteritis H: Diarrhea lasting >2 weeks (e.g., post-infectious diarrhea).
Inflammatory Bowel Disease (IBD) H: Bloody diarrhea, abdominal pain, and weight loss.
Idiopathic Thrombocytopenic Purpura (ITP) H: Petechiae onset 1-4 weeks after a viral illness in a well child.
Viral Infections H: Non-specific prodrome of fever, malaise, or rash.
Invasive Meningococcal Disease H: Rapid progression of fever, headache, and toxicity.
Henoch-Schönlein Purpura (HSP) / IgA Vasculitis H: History of recent URTI; onset of colicky abdominal pain and joint pain.
Osteomyelitis H: Localized bone pain that is constant and worse at night.
Septic Arthritis H: Acute onset of a refusal to bear weight on a single joint.
Pyomyositis H: Painful swelling of a large muscle group; often in a tropical climate.
Discitis H: Refusal to sit, stand, or walk (or abdominal/back pain) in a young child.
Viral Meningitis H: Headache, fever, and neck stiffness, but non-toxic appearance.
Bacterial Meningitis H: Acute onset of high fever, confusion, and lethargy; potentially recent ear/sinus infection.
Encephalitis H: Symptoms of an acute illness followed by altered mental status or personality change.
Brain Abscess H: Symptoms often subtle/subacute; history of chronic ear/sinus infection.
Global Developmental Delay (of unknown cause) H: Delay in two or more developmental domains (e.g., motor and language).
Intellectual Disability H: Poor academic performance/learning ability; difficulties with adaptive skills.
Autism Spectrum Disorder (ASD) H: Difficulties with social communication and interaction; restricted/repetitive behaviors.
Genetic Syndromes (e.g., Down Syndrome) H: Prenatal/early genetic diagnosis or family history.
New Diagnosis of Type 1 Diabetes Mellitus (T1DM) H: Polyuria, polydipsia, and weight loss over several weeks/months.
Omission/Interruption of Insulin Therapy H: Known T1DM; history of missing insulin doses or pump malfunction.
Acute Infection/Illness H: Recent or current illness (e.g., flu, UTI) as the trigger for DKA.
Poor Metabolic Control H: Known T1DM; history of consistently high blood sugars.
Phenylketonuria (PKU) H: Normal at birth, then gradual development of developmental delay/seizures.
Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) H: Acute illness (lethargy, vomiting) precipitated by fasting or infection.
Urea Cycle Disorders H: Onset of symptoms (lethargy, vomiting) after protein feeding.
Lysosomal Storage Disorders H: Progressive neurological deterioration and/or organ enlargement.
Oligoarticular JIA H: Arthritis affecting **<5 joints** during the first 6 months.
Polyarticular JIA (RF Negative) H: Arthritis affecting more than 5 joints** during the first 6 months; no rheumatoid factor.
Enthesitis-related Arthritis (ERA) H: Lower limb arthritis associated with pain at tendon insertion sites (enthesitis).
Systemic JIA (Still's Disease) H: Arthritis preceded/accompanied by a high, quotidian (once-daily) fever for more than 2 weeks
Spastic Cerebral Palsy (most common) H: History of prematurity or perinatal brain injury (e.g., PVL).
Mixed Cerebral Palsy H: History of mixed movement types.
Athetoid (Dyskinetic) Cerebral Palsy H: History of severe neonatal jaundice (kernicterus) or acute asphyxia.
Ataxic Cerebral Palsy H: Difficulty with coordination and balance.
Cerebral Palsy H: Fixed, non-progressive neurological impairment; motor delay.
Down Syndrome H: Prenatal/Genetic diagnosis.
Muscular Dystrophy H: Progressive motor weakness; difficulty climbing stairs/getting up.
Prader-Willi Syndrome H: Infantile feeding difficulties and failure to thrive (early), progressing to severe hyperphagia (later).
Group B Streptococcus (GBS) H: Early onset (within 7 days) in a mother without GBS prophylaxis.
Escherichia coli (E. coli) H: Often late onset; associated with prematurity or urinary tract infection.
Listeria monocytogenes H: Mother consumed contaminated food (deli meat, unpasteurized cheese).
Coagulase-negative Staphylococci (CoNS) H: Associated with indwelling lines (IV, central catheter).
Minimal Change Disease (Nephrotic Syndrome) H: Acute onset of puffy eyes (periorbital edema).
Post-infectious Glomerulonephritis (Nephritic Syndrome) H: Onset 1-3 weeks after a strep throat or skin infection.
Focal Segmental Glomerulosclerosis (FSGS) H: Steroid resistance or relapse after initial steroid therapy.
IgA Nephropathy H: Onset of gross hematuria coincident with a viral upper respiratory infection.
Common Cold H: Gradual onset of clear rhinorrhea and sore throat.
Bronchiolitis (RSV) H: Cough and respiratory distress following 1-3 days of cold symptoms, in a child <2 years old.
Croup (Laryngotracheobronchitis) H: Onset of a fever and a characteristic "barking" cough (often worse at night).
Pneumonia H: Persistent cough, fever, and tachypnea; often with chest pain.
Lupus Nephritis H: History of SLE; unexplained edema or bubbly urine.
Arthritis/Arthralgia H: Joint pain/stiffness, especially in the morning.
Hematologic Disorders H: Unexplained fatigue, easy bruising, or recurrent infections.
Malar Rash/Photosensitivity H: History of a facial rash, often after sun exposure.
Created by: MeanHeem
 

 



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