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21hydroxylasedeficiency chronic classification diagnosis disorders endocrinology genetics pediatrics peds veins venous
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
CEAP Classification of Chronic Venous Disorders Clinical: C0 - NO clinical signs C1 - Small
CEAP Classification ... : C0 - NO clinical ... signs C1 - Small ... Perforating veins Pathophysiology ... Obstruction #CEAP
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