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常染色体显性多囊肾病的产前发病

Prenatal onset of autosomal dominant polycystic kidney disease.

作者信息

Edwards O P, Baldinger S

机构信息

Department of Pathology, Minneapolis Children's Medical Center, Minnesota.

出版信息

Urology. 1989 Nov;34(5):265-70. doi: 10.1016/0090-4295(89)90322-1.

Abstract

Autosomal dominant polycystic kidney disease presenting in the fetus or newborn is rare, only 22 cases having been reported in the literature. A case is reported of a premature newborn infant with severe renal involvement and extrarenal associated abnormalities. The literature is reviewed, and the importance of considering this entity in infants with polycystic kidney disease is discussed since it may affect both genetic counseling and surgical management when radiographically detected.

摘要

胎儿期或新生儿期出现的常染色体显性多囊肾病很罕见,文献中仅报道过22例。本文报告了1例患有严重肾脏受累及肾外相关异常的早产新生儿病例。对相关文献进行了综述,并讨论了在患有多囊肾病的婴儿中考虑这一疾病实体的重要性,因为当通过影像学检查发现时,它可能会影响遗传咨询和手术治疗。

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