Back to Search Start Over

Autosomal recessive polycystic kidney disease.

Authors :
Zerres K
Rudnik-Schöneborn S
Steinkamm C
Becker J
Mücher G
Source :
Journal of molecular medicine (Berlin, Germany) [J Mol Med (Berl)] 1998 Apr; Vol. 76 (5), pp. 303-9.
Publication Year :
1998

Abstract

Autosomal recessive polycystic kidney disease (ARPKD) is a rare inherited disorder which usually becomes clinically manifest in early childhood, although the spectrum of ARPKD is much more variable than generally known. Presentation of ARPKD at later ages and survival into adulthood have been observed in many cases. The responsible gene has been mapped to chromosome 6p. Thus there is no evidence of genetic heterogeneity. The most important indication for DNA diagnosis is the prenatal diagnosis in families with at least one affected child. The critical region has been narrowed with the use of recombinant families of about 4 cM. Several possible candidate genes have been excluded.

Details

Language :
English
ISSN :
0946-2716
Volume :
76
Issue :
5
Database :
MEDLINE
Journal :
Journal of molecular medicine (Berlin, Germany)
Publication Type :
Academic Journal
Accession number :
9587064
Full Text :
https://doi.org/10.1007/s001090050221