UPMC Université Paris 06, Paris, France.
Reprod Biomed Online. 2012 Apr;24(4):462-5. doi: 10.1016/j.rbmo.2011.12.008. Epub 2012 Jan 8.
Müllerian agenesis, also termed the Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS) is a disorder with an incidence of approximately 1 in 4500 newborn girls. This study screened 12 patients with MRKHS for mutations in two genes, LAMC1 and DLGH1, involved in the development of Müllerian structures and found 10 previously described variants and no novel variants in the coding sequence. It is highly unlikely that these variants are pathological since these are common in the general population. It is the first time that an extensive study of LAMC1 and DLGH1 has been undertaken in patients with MRKHS. The data support the notion that mutations in the coding sequence of LAMC1 and DLGH1 may not be associated with MRKHS.
米勒管发育不全,也称为梅耶-罗基坦斯基-库斯特-豪泽综合征(MRKHS),是一种发病率约为每 4500 名新生女婴中出现 1 例的疾病。本研究对 12 例 MRKHS 患者的两个基因 LAMC1 和 DLGH1 进行了突变筛查,在编码序列中发现了 10 个先前描述的变异体和 0 个新的变异体。这些变异体很可能不是病理性的,因为它们在普通人群中很常见。这是首次在 MRKHS 患者中对 LAMC1 和 DLGH1 进行广泛的研究。这些数据支持这样一种观点,即 LAMC1 和 DLGH1 编码序列中的突变可能与 MRKHS 无关。