CONGENITAL BILATERAL ABSENCE OF THE VAS-DEFERENS AND CYSTIC-FIBROSIS

被引：0

作者：

KUGLER, A

LACCONE, F

WEIDNER, W

KALLERHOFF, M

机构：

[1] UNIV GOTTINGEN,INST HUMANGENET,W-3400 GOTTINGEN,GERMANY

[2] UNIV GIESSEN,UROL KLIN,W-6300 GIESSEN,GERMANY

来源：

UROLOGE-AUSGABE A | 1995年 / 34卷 / 04期

关键词：

CONGENITAL ABSENCE OF THE VAS DEFERENS; CYSTIC FIBROSIS; MALE INFERTILITY;

D O I：

暂无

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Aspermia caused by absence of the vas deferens is well known in cystic fibrosis. It has been suggested that otherwise healthy males with congenital bilateral absence of the vas deferens (CBAVD), which was previously considered a distinct genetic entity, have an increased frequency of CF gene mutations. CBAVD is now considered to be a mild form of cystic fibrosis. We report the case of an azoospermic man who had undergone exploratory scrototomy because of aplasia of the epididymis and vas deferens. Genetic screening for cystic fibrosis revealed a compound heterozygote for CFTR mutations Delta F 508 and R 117 H.

引用

页码：348 / 350

页数：3

共 50 条

[1] CONGENITAL BILATERAL ABSENCE OF THE VAS-DEFERENS AND CYSTIC-FIBROSIS
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[2] CONGENITAL BILATERAL ABSENCE OF VAS-DEFERENS IN ABSENCE OF CYSTIC-FIBROSIS
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