| Literature DB >> 3681905 |
K D MacDermot1, S C Roth, C Hall, R M Winter.
Abstract
A family is presented with short stature, femoral epiphyseal dysplasia, mild vertebral changes, and sensorineural deafness inherited as an autosomal dominant trait. Myopia and retinal detachment presenting in adult life were also present in some affected members. We suggest that this disorder may be a distinct entity within the spondyloepiphyseal dysplasia group of disorders.Entities:
Mesh:
Year: 1987 PMID: 3681905 PMCID: PMC1050287 DOI: 10.1136/jmg.24.10.602
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318