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近来,显性遗传性多囊肾病(PKD)婴儿病例报告增多。本文通过回顾性研究,分析了1岁内发病的儿童PKD病例中隐性和显性型的相关性,普通放射线检查方法鉴别隐性和显性PKD的可能性及儿童PKD在幼儿期的自然转归。方法分析1970～1984年出生的儿童PKD病例,1岁内确诊并至少生存1个月者列入研究对象,分成常染色体隐性遗传性PKD(下称隐性)、常染
Recently, there have been reports of infantile cases of overt genetic polycystic kidney disease (PKD). In this retrospective study, we analyzed the relationship between recessive and dominant type in childhood PKD patients within 1 year of age, the possibility of distinguishing between latent and dominant PKD by ordinary radiological examination and the natural transition of childhood PKD in early childhood Return Methods The children with PKD who were born between 1970 and 1984 were analyzed. Patients diagnosed within 1 year of age and at least one month survived were included in the study. Patients were divided into autosomal recessive inherited PKD (implicit)