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Autosomal dominant polycystic disease

✍ Scribed by Carlo Pedrolli; Emanuele Cereda


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
112 KB
Volume
50
Category
Article
ISSN
0270-9139

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✍ Dr. A. Dobin; W. J. Kimberling; W. Pettinger; J. E. Bailey-Wilson; Y. Y. Shugart πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 785 KB

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

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We evaluated the accuracy of ultrasonographic diagnosis of autosomal dominant polycystic kidney disease (ADPKD) and factors influencing its prognosis in members of 17 Newfoundland families originally described in 1984. In 10 families showing genetic linkage between ADPKD and markers for the PKDl loc

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Autosomal dominant polycystic kidney disease (ADPKD) arises from mutations in the PKD1 and PKD2 genes. The Polycystic Kidney Disease Mutation Database (PKDB) is an internet-accessible relational database containing comprehensive information about germline and somatic disease-causing variants within

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Multiple, bilateral seminal vesicle cysts were found in a young man by transabdominal sonography. Examination of the kidneys disclosed previously unknown autosomal dominant polycystic kidney disease. This case report draws attention to the rare association between these 2 conditions.