Latini G, Caliandro P
Divisione di Pediatria, Ospedale Regionale A. di Summa, U.S.L. BR/4, Brindisi, Italia.
Pediatr Med Chir. 1991 Jan-Feb;13(1):95-6.
After presenting the personal case, the authors describe the main features of the autosomally recessive polycystic disease with kidney and hepatic involvement and a variety of clinical expressions. Diagnosis is based on genetic study, instrumental examinations and histological data.
在介绍了个人病例后，作者描述了伴有肾脏和肝脏受累及多种临床表现的常染色体隐性多囊病的主要特征。诊断基于基因研究、影像学检查和组织学数据。
