late pathophysiology difficult treatment endocrinology peds differential 21ohd acromegaly

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

, vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics

Acromegaly - Diagnosis and Management Summary - GrepMed Handbook

Clinical Presentation:
• Classic Acromegaly: frontal

Acromegaly - Diagnosis ... malignancy Pathophysiology ... Differential Diagnosis ... Diagnosis #Management #Endocrinology ... #Treatment #Pathophysiology

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