The attitude of Japanese physicians regarding genetic service for autosomal dominant polycystic kidney disease (ADPKD)
โ Scribed by Shinsuke Nomura; Shin-ichiro Kawai; Tatsuo Fukushima; Hirotaka Katoh; Gengo Osawa
- Book ID
- 105391811
- Publisher
- Nature Publishing Group
- Year
- 1994
- Tongue
- English
- Weight
- 265 KB
- Volume
- 39
- Category
- Article
- ISSN
- 1435-232X
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๐ SIMILAR VOLUMES
## Background: Autosomal-dominant polycystic kidney disease (adpkd) is characterized by gradual renal enlargement and cyst growth prior to loss of renal function. standard radiographic imaging has not provided the resolution and accuracy necessary to detect small changes in renal volume or to relia
Polycystic kidney disease (PKD) is a common autosomal dominant genetic disorder caused by mutation in at least two different gene loci. The PKD1 gene has been localized on the short arm of chromosome 16. The location of a second genetic locus in the human genome is not yet known. A large PKD kindred