| Literature DB >> 2650933 |
E M Williams1, A C Nicholls, S C Daw, N Mitchell, L S Levin, B Green, J MacKenzie, D R Evans, P A Chudleigh, F M Pope.
Abstract
Severe Sillence type II/III Osteogenesis imperfecta (OI) is a lethal or severely crippling disease with either autosomal dominant or recessively inherited type I collagen mutations. Here we describe the detailed clinical features of a thin-ribbed OI variant with deformed limbs. The three consecutively affected children showed no genetic linkage with either of the two type I collagen genes, which implies that a novel mechanism causes this clinical phenotype. It can be prevented using ultrasound to diagnose affected foetuses.Entities:
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Year: 1989 PMID: 2650933 DOI: 10.1111/j.1399-0004.1989.tb02926.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438