17 alpha-hydroxylase deficiency physical examination

Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency Microchapters
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Differentiating Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency from other Diseases
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]

Overview

Patients with congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency usually appear general appearance. Physical examination of patients with congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency is usually remarkable for gynaecomastia, hypertension, and sexual infantilism.

Physical Examination

Appearance of the Patient

• Gynaecomastia

Vital Signs

• Hypertension

Genitourinary

• Sexual infantilism
• No pubic or axillary hair