Identification of a novel mutation in exon 1 of androgen receptor gene in an azoospermic patient with mild androgen insensitivity syndrome: case report and literature review.

Objective: To report a case of an azoospermic subject with mild androgen insensitivity syndrome (MAIS) and review the relevant literature.

Methods: Case report. Methods: Academic research hospital. Methods: A 49-year-old man with undermasculinized features and a history of cryptorchidism and azoospermia. Methods: Hormonal evaluation and genetic testing of the androgen receptor gene (AR). Methods: Hormonal levels and sequence chromatogram of the proband and his mother.

Results: We found total T in the normal range and high levels of gonadotropins. Karyotype was 46,XY. Genetic testing identified a novel mutation of exon 1 of AR, which resulted in an alanine to serine substitution in the transactivation domain at codon 240 (A240S). Fourteen other mutations of exon 1 of AR have been associated with MAIS to date.

Conclusions: The novel mutation A240S of AR is involved in MAIS, a syndrome associated with azoospermia.