infertility nejm honc pathophysiology clinical egd genetics 21ohd diagnosis - GrepMed

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2 results

21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

Pathogenesis and Clinical ... Hirsutism & acne • Infertility ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology

IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings

- Infectious Agents - 50% have

Pathogenesis and Clinical ... predisposition - Various genetic ... galactose-deficient IgA1 (GD-IgA1 ... HenochScholeinPurpura #Pathophysiology ... #Diagnosis #Signs

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