Association of congenital hepatic fibrosis with autosomal dominant polycystic kidney disease
โ Scribed by B. Lipschitz; W. E. Berdon; A. R. Defelice; J. Levy
- Publisher
- Springer-Verlag
- Year
- 1993
- Tongue
- English
- Weight
- 830 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0301-0449
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The results of classical segregation analysis on 159 families with polycystic kidney disease (PKD) are presented. It had been previously estimated that about 95% of autosomal dominant PDK (ADPKD) families have PKD 1, the gene localized to chromosome 16p. The main purpose of the study was to determin
The goal of this study was to determine whether use of postmenopausal estrogen (Premarin, Wyeth-Ayerst, Philadelphia, PA) in women with autosomal dominant polycystic kidney disease (ADPKD) increases liver, hepatic cyst, or kidney volume. We also determined whether clinical symptoms correlated with t
Hepatic cysts are a major manifestation of autosomal dominant polycystic kidney disease. This study examined 239 autosomal dominant polycystic kidney disease patients and 189 unaffected family members to define the factors that influence the presence and severity of hepatic cysts. Autosomal dominant