Autosomal recessive polycystic kidney disease: mapping to chromosomal region of 6p21-cen in a Turkish child

Autosomal recessive polycystic kidney disease (ARPCD) is a congenital kidney disease with severe prognosis. We present a male infant who was diagnosed prenatally by ultrasonography. He died at two months of age in a septic stage. The genetic defect for ARPCD has been mapped to chromosomal reg...

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Bibliographic Details
Main Authors: N Beşbaş, S Ozen, U Saatçi, M Cağlar, G Mucher, K Zerres
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 1998-04-01
Series:The Turkish Journal of Pediatrics
Online Access:https://turkjpediatr.org/article/view/3306
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