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diagnosis signs 21hydroxylasedeficiency 21ohd henochscholeinpurpura iga pediatrics peds psychiatry vasculitis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings - Infectious Agents - 50% have
predisposition - Various genetic ... nephrotic/nephritic syndrome ... and ankles) #HSP ... HenochScholeinPurpura #Pathophysiology ... Diagnosis #Signs #Symptoms
Serotonin Syndrome: Pathogenesis and Clinical Findings Serotonin Syndrome: Variable combination of mental status changes, autonomic instability, and
Serotonin Syndrome ... ingestion and most cases ... muscle rigidity (esp ... #Syndrome #Pathophysiology ... Diagnosis #Signs #Symptoms
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