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21hydroxylasedeficiency endocrinology features genetics kawasaki pathophysiology sepsis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... endocrinology #peds ... #pediatrics
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Kawasaki Disease ... immunoglobulin reduces the risk ... #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
Pediatrics Sepsis Screening SIGNS OF INFECTION? • Fever (>38C) • Hypothermia (<36C) • Cough/chest pain/respiratory distress •
Pediatrics Sepsis ... Screening SIGNS ... neuromuscular disease ... #Pediatrics #peds ... #diagnosis
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