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21hydroxylasedeficiency clinical galant genetics neurology normal physicalexam primitive reflex
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Galant Reflex on Physical Exam The Galant reflex is present at birth and remains until the 2nd
study, where the pelvis ... persistent in cases ... PhysicalExam #clinical #video ... #Neurology #Peds ... #Pediatrics #Normal
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