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peds diagnosis 21hydroxylasedeficiency 21ohd differential disease endocrinology examination genetics incomplete kawasaki newborn physicalexam
Causes of anemia in infants & children #Diagnosis #Peds #Pediatrics #Differential #Anemia #Causes #Algorithm
Causes of anemia ... in infants & children ... Diagnosis #Peds #Pediatrics ... #Differential #Anemia ... #Causes #Algorithm
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... 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 ... clinical and lab signs ... Diagnosis #Peds #Pediatrics
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... is also a late sign ... are observed for signs ... intra-abdominal masses ... Examination #Peds #Pediatrics
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