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21hydroxylasedeficiency diagnosis endocrinology genetics hematology management pathophysiology peds polycythemiavera pv summary
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
occur in utero as ... Signs/Symptoms/Complications ... Labia major & minor ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds #pediatrics
Polycythemia Vera (PV) - Diagnosis and Management Summary Diagnostic Criteria: • Elevated hemoglobin and/or hematocrit AND •
When present, symptoms ... , signs, and complications ... : • As with ET ... • Treatment algorithms ... #hematology
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