2 results
21hydroxylasedeficiency 21ohd diagnosis endocrinology genetics henochschonleinpurpura hsp igav
Diagnosis of IgA Vasculitis (Henoch-Schönlein Purpura) - French Vasculitis Study Group 1) Suggestive clinical manifestations
potential severe complications ... especially in the skin ... arterioles in the skin ... HSP #Diagnosis #Rheumatology ... #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics
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