常染色体隐性遗传性多囊肾又称婴儿型多囊肾，为多囊肾中少见类型。
Autosomal recessive polycystic kidney disease also known as infantile polycystic kidney disease, polycystic kidney in the rare type.
婴儿型多囊肾又叫常染色体隐性遗传型多囊肾，是两种多囊肾中的一种。
Infantile polycystic kidney disease and autosomal recessive polycystic kidney disease, is the two kind of polycystic kidney in a kind.
常染色体隐性遗传型多囊肾的病因主要是因为父母先天性的遗传，所以在婴儿期就开始发病。
Autosomal recessive polycystic kidney disease etiology is mainly because the parents with congenital genetic, so in infancy began to sicken.
目的研究常染色体显性遗传型多囊肾病肾组织中细胞外基质和多囊蛋白-1的表达及与囊肿发生的关系。
Objective To study the expression of extracellular matrix and polycystin-1 in ADPKD and their relation to cyst formation.
目的：研究华东地区汉族人常染色体显性遗传性多囊肾病(adpkd)基因型与临床表现型的关系。
Objective: to analyze the relationship between the genotype and phenotype of autosomal dominant polycystic kidney disease (ADPKD) in Han nationality in East China.
目的：研究华东地区汉族人常染色体显性遗传性多囊肾病(adpkd)基因型与临床表现型的关系。
Objective: to analyze the relationship between the genotype and phenotype of autosomal dominant polycystic kidney disease (ADPKD) in Han nationality in East China.
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