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常染色体显性多囊肾病基因决定的早期表现的产前诊断?

Prenatal diagnosis of genetically determined early manifestation of autosomal dominant polycystic kidney disease?

作者信息

Zerres K, Hansmann M, Knöpfle G, Stephan M

出版信息

Hum Genet. 1985;71(4):368-9. doi: 10.1007/BF00388467.

Abstract

A case of an unusually early manifestation of autosomal dominant polycystic kidney disease (ADPKD) is reported that was prenatally diagnosed by ultrasound. The ultrasonographic picture showed greatly enlarged kidneys and increased echogenicity that was indistinguishable from cases of autosomal recessive polycystic kidney disease or Meckel syndrome without further information. Because of two further cases of early manifestation of ADPKD within the family reported (brother and cousin), as well as several other "familial" cases reported in the literature, we postulate that genetic factors are involved (modifying alleles). When reported observations of "familial" cases of early manifestations of ADPKD are made, genetic counseling should be considered.

摘要

报告了一例常染色体显性多囊肾病(ADPKD)异常早期表现的病例,该病例通过超声在产前被诊断出来。超声图像显示肾脏显著增大且回声增强,在没有更多信息的情况下,这与常染色体隐性多囊肾病或梅克尔综合征的病例难以区分。由于该家族中另外报告了两例ADPKD早期表现的病例(兄弟和堂兄弟),以及文献中报道的其他几例“家族性”病例,我们推测遗传因素(修饰等位基因)参与其中。当报告ADPKD早期表现的“家族性”病例的观察结果时,应考虑进行遗传咨询。

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