| Literature DB >> 9237505 |
S Kurtoglu1, M Dundar, I K Hallaç, K Uzüm, Y Okumuş, T Oktem.
Abstract
Larsen's syndrome is characterised by multiple joint dislocations, flat face and talipes equinovarus. There is an autosomal dominant form and also a more severe autosomal recessive form. Several types of polycystic kidney disease have been reported in children. In this report we present an infant with a severe form of Larsen's syndrome (thought to be lethal Larsen-like), infantile-type polycystic kidney disease, biliary dysgenesis and osteosclerosis.Entities:
Mesh:
Year: 1997 PMID: 9237505 DOI: 10.1111/j.1399-0004.1997.tb02500.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438