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21hydroxylasedeficiency causes differential disease endocrinology genetics incomplete kawasaki pathophysiology
Causes of anemia in infants & children #Diagnosis #Peds #Pediatrics #Differential #Anemia #Causes #Algorithm
Causes of anemia ... in infants & children ... #Diagnosis #Peds ... #Pediatrics #Differential ... #Algorithm
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
Evaluation of suspected incomplete Kawasaki Disease 1. AHA consensus recommendations 2. Infants ≤6 months old on day ≥7
Infants ≤6 months ... Albumin ≤3.0 g/dL, anemia ... purposes of this algorithm ... #Diagnosis #Peds ... #Pediatrics #Kawasaki
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