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21ohd diagnosis endocrinology genetics hematology pathophysiology pediatrics polycythemia workup
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... as males at birth ... decr feeding, weight ... a scrotum #21HydroxylaseDeficiency ... endocrinology #peds
Polycythemia - Differential Diagnosis Algorithm Polycythemia itself isn’t a diagnosis. Like many things, it is a condition
Polycythemia - Differential ... Diagnosis Algorithm ... dL, Hct>49% - Female ... Look back in the chart ... levels: normal/high
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