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Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibships

✍ Scribed by F. Deget; S. Rudnik-Schöneborn; K. Zerres

Book ID: 115091769
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 493 KB
Volume: 47
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.1995.tb04305.x

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Autosomal recessive polycystic kidney disease (ARPKD) is one of the most common hereditary renal cystic diseases and has a high infant mortality. Prenatal diagnosis using fetal sonography can be unreliable, especially in early pregnancy. The ARPKD locus has been mapped to proximal chromosome 6p allo