7 results
21hydroxylasedeficiency 21ohd algorithm alkaptonuria anomalous blackurine cardiology disease endocrinology examination genetics incomplete infant kawasaki management newborn otitismedia physicalexam pulmonary return
Total Anomalous Pulmonary Venous Return (TAPVR) • Introduction • Classification • Pathophysiology of TAPVR • Presentation
Classification • Pathophysiology ... PVO Present • Diagnosis ... Classic “snowman sign ... management #cardiology #peds ... #pediatrics #summary
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... non-arousable, decr urine ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
Alkaptonuria (Black Urine Disease) Urine turns dark when left standing due to oxidation of homogentisic acid Clinical
Alkaptonuria (Black Urine ... Disease) Urine ... Alkaptonuria #BlackUrine #Peds ... #Pediatrics #Diagnosis ... #Pathophysiology
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
#OtitisMedia #pathophysiology ... #diagnosis #symptoms ... #signs #peds #pediatrics
Pediatrics Sepsis Screening SIGNS OF INFECTION? • Fever (>38C) • Hypothermia (<36C) • Cough/chest pain/respiratory distress •
Pediatrics Sepsis ... Screening SIGNS ... • ↓ feeding, ↓ urine ... Sepsis #Screening #Pediatrics ... #peds #diagnosis
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
15,000/mm3, and urine ... clinical and lab signs ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
pressure and cranial ultrasound ... is also a late sign ... When the diagnosis ... #Examination #Peds ... #Pediatrics #Diagnosis
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