Novel point mutations in complete androgen insensitivity syndrome with incomplete müllerian regression: Two Taiwanese patients

Yang H. Van, Ju L. Lin, Shiu Feng Huang, Chih Cheng Luo, Chen Sheng Hwang, Fu Sung Lo

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Complete androgen insensitivity syndrome (CAIS) is a relatively rare X-linked disorder caused by androgen receptor gene (AR) mutations that result in complete impairment of genital virilisation. In these individuals, no müllerian derivatives are usually found; however, several sporadic cases of CAIS with müllerian remnants have been reported. In this paper, we report two novel point mutations of the AR gene resulting in two cases of CAIS with incomplete müllerian regression. Molecular studies of cases 1 and 2 showed novel missense mutations of the AR gene, with a methionine to threonine substitution at codon 749 (base 2608 T → C) in exon 5 and a methionine to lysine substitution at codon 787 (base 2722 T → A) in exon 6. Both patients received bilateral gonadectomy and inguinal hernia repair. The excised gonads proved to be testes with incomplete regression of the müllerian structures. Conclusion: Müllerian structures can be present in androgen insensitivity syndrome and the presence of a uterus therefore does not exclude this disorder. Further study of these patients may promote a better understanding of the pathogenesis.

Original languageEnglish
Pages (from-to)781-784
Number of pages4
JournalEuropean Journal of Pediatrics
Volume162
Issue number11
DOIs
Publication statusPublished - Nov 2003
Externally publishedYes

Fingerprint

Androgen-Insensitivity Syndrome
Point Mutation
Androgen Receptors
Genes
Codon
Methionine
Exons
Virilism
Inguinal Hernia
Herniorrhaphy
Gonads
Missense Mutation
Threonine
Lysine
Uterus
Testis
Mutation

Keywords

  • Androgen insensitivity syndrome
  • Androgen receptor
  • Complete androgen insensitivity syndrome
  • Partial androgen insensitivity syndrome
  • Testicular feminisation

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Novel point mutations in complete androgen insensitivity syndrome with incomplete müllerian regression : Two Taiwanese patients. / Van, Yang H.; Lin, Ju L.; Huang, Shiu Feng; Luo, Chih Cheng; Hwang, Chen Sheng; Lo, Fu Sung.

In: European Journal of Pediatrics, Vol. 162, No. 11, 11.2003, p. 781-784.

Research output: Contribution to journalArticle

Van, Yang H. ; Lin, Ju L. ; Huang, Shiu Feng ; Luo, Chih Cheng ; Hwang, Chen Sheng ; Lo, Fu Sung. / Novel point mutations in complete androgen insensitivity syndrome with incomplete müllerian regression : Two Taiwanese patients. In: European Journal of Pediatrics. 2003 ; Vol. 162, No. 11. pp. 781-784.
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