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| Question | Answer |
|---|---|
| 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. |