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先天性输精管缺失的遗传学研究。

Genetics of the congenital absence of the vas deferens.

机构信息

Service de Génétique Médicale, Hôpital Purpan, CHU, 31059, Toulouse, France.

Service de Biochimie, Institut Fédératif de Biologie, CHU, 31059, Toulouse, France.

出版信息

Hum Genet. 2021 Jan;140(1):59-76. doi: 10.1007/s00439-020-02122-w. Epub 2020 Feb 5.

Abstract

Congenital absence of the vas deferens (CAVD) may have various clinical presentations depending on whether it is bilateral (CBAVD) or unilateral (CUAVD), complete or partial, and associated or not with other abnormalities of the male urogenital tract. CBAVD is usually discovered in adult men either during the systematic assessment of cystic fibrosis or other CFTR-related conditions, or during the exploration of isolated infertility with obstructive azoospermia. The prevalence of CAVDs in men is reported to be approximately 0.1%. However, this figure is probably underestimated, because unilateral forms of CAVD in asymptomatic fertile men are not usually diagnosed. The diagnosis of CAVDs is based on clinical, ultrasound, and sperm examinations. The majority of subjects with CAVD carry at least one cystic fibrosis-causing mutation that warrants CFTR testing and in case of a positive result, genetic counseling prior to conception. Approximately 2% of the cases of CAVD are hemizygous for a loss-of-function mutation in the ADGRG2 gene that may cause a familial form of X-linked infertility. However, despite this recent finding, 10-20% of CBAVDs and 60-70% of CUAVDs remain without a genetic diagnosis. An important proportion of these unexplained CAVDs coexist with a solitary kidney suggesting an early organogenesis disorder (Wolffian duct), unlike CAVDs related to CFTR or ADGRG2 mutations, which might be the result of progressive degeneration that begins later in fetal life and probably continues after birth. How the dysfunction of CFTR, ADGRG2, or other genes such as SLC29A3 leads to this involution is the subject of various pathophysiological hypotheses that are discussed in this review.

摘要

先天性输精管缺如(CAVD)可能有各种临床表现,具体取决于其是双侧(CBAVD)还是单侧(CUAVD)、完全性还是不完全性,以及是否伴有男性泌尿生殖道的其他异常。CBAVD 通常在成年男性中发现,要么是在对囊性纤维化或其他 CFTR 相关疾病进行系统评估时,要么是在对伴有梗阻性无精子症的孤立性不育症进行检查时。CAVD 男性的患病率约为 0.1%。然而,这个数字可能被低估了,因为无症状生育男性的单侧 CAVD 通常不会被诊断出来。CAVD 的诊断基于临床、超声和精液检查。大多数 CAVD 患者至少携带一种导致 CFTR 检测的囊性纤维化致病突变,如果结果阳性,在受孕前需要进行遗传咨询。CAVD 病例中约有 2%是 ADGRG2 基因无功能突变的半合子,可能导致 X 连锁的家族性不育症。然而,尽管有了这一最新发现,10-20%的 CBAVD 和 60-70%的 CUAVD 仍然没有遗传诊断。这些未解释的 CAVD 中有很大一部分与孤立肾并存,提示存在早期器官发生障碍(沃尔夫管),与 CFTR 或 ADGRG2 突变相关的 CAVD 不同,这些突变可能是胎儿生命后期开始的进行性退化的结果,并且可能在出生后仍在继续。CFTR、ADGRG2 或 SLC29A3 等其他基因的功能障碍如何导致这种退化是各种病理生理学假说的主题,本文对此进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76d1/7864840/b43e3223dd80/439_2020_2122_Fig1_HTML.jpg

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