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Dokumenttyp:
Journal Article; Article
Autor(en):
Hoefele, Julia; Mayer, Karin; Marschall, Christoph; Alberer, Martin; Klein, Hanns-Georg; Kirschstein, Martin
Titel:
Rare co-occurrence of osteogenesis imperfecta type I and autosomal dominant polycystic kidney disease.
Abstract:
There are several clinical reports about the co-occurrence of autosomal dominant polycystic kidney disease (ADPKD) and connective tissue disorders. A simultaneous occurrence of osteogenesis imperfecta (OI) type I and ADPKD has not been observed so far.This report presents the first patient with OI type I and ADPKD.Mutational analysis of PKD1 and COL1A1 in the index patient revealed a heterozygous mutation in each of the two genes. Mutational analysis of the parents indicated the mother as a carr...     »
Zeitschriftentitel:
World J Pediatr
Jahr:
2016
Band / Volume:
12
Heft / Issue:
4
Seitenangaben Beitrag:
501-503
Sprache:
eng
Volltext / DOI:
doi:10.1007/s12519-016-0014-1
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/27059743
Print-ISSN:
1708-8569
TUM Einrichtung:
Institut für Humangenetik
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