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

研究成果: 雜誌貢獻文章

17 引文 斯高帕斯(Scopus)

摘要

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.

原文英語
頁(從 - 到)781-784
頁數4
期刊European Journal of Pediatrics
162
發行號11
DOIs
出版狀態已發佈 - 十一月 2003
對外發佈Yes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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