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partial enzyme deficiency causing excess androgen production

Non-Classical Adrenal Hyperplasia (NCAH) is a milder form of congenital adrenal hyperplasia that typically presents later in life, often during adolescence or adulthood. It is caused by a partial deficiency in the enzyme 21-hydroxylase, leading to an overproduction of androgens (male hormones). Symptoms can include irregular menstrual cycles, excessive hair growth (hirsutism), and acne in females, while males may experience early signs of puberty.

Related Terms

• Congenital Adrenal Hyperplasia
• Classic Congenital Adrenal Hyperplasia
• Adrenal Hyperplasia
• CAH
• Classical Congenital Adrenal Hyperplasia
• Classic Adrenal Hyperplasia
• 21-Hydroxylase Deficiency