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常染色体显性遗传性多囊肝病:另一家系

Autosomal dominant polycystic liver disease: a second family.

作者信息

Berrebi G, Erickson R P, Marks B W

出版信息

Clin Genet. 1982 May;21(5):342-7. doi: 10.1111/j.1399-0004.1982.tb01381.x.

Abstract

An autosomal dominant pattern of transmission has been established for polycystic kidney disease. The degree of cystic involvement of other organs has been variable. The genetic pattern of transmission of polycystic liver disease independent of cystic kidney disease has never been established. We present a second family with polycystic liver disease without kidney disease. The lack of renal cysts is unlikely to be due to variable expressivity and penetrance of the gene for polycystic kidney disease. The liver cysts may be of late onset since none of the proband's four children demonstrate cysts. Alternatively, none of these four individuals may have received the gene for polycystic liver disease from their affected mother. The family described supports an autosomal dominant pattern of inheritance for polycystic liver disease.

摘要

多囊肾病已确定为常染色体显性遗传模式。其他器官的囊性受累程度各不相同。独立于多囊肾病的多囊肝病的遗传模式尚未确定。我们报告了第二个患有无肾病的多囊肝病家族。肾囊肿的缺失不太可能是由于多囊肾病基因的可变表达和外显率所致。肝囊肿可能是迟发性的,因为先证者的四个孩子均未显示囊肿。或者,这四个个体中没有一个可能从其患病母亲那里获得多囊肝病基因。所描述的这个家族支持多囊肝病的常染色体显性遗传模式。

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