| Literature DB >> 8487283 |
W Reardon1, N Lewis, H E Hughes.
Abstract
Genetic counselling in the autosomal dominant condition of the Romano-Ward syndrome might be assumed to be relatively straightforward. The problems posed by consanguinity, deafness, and subclinical gene carriers in a pedigree with this condition have caused us to reevaluate this view. The diagnostic and management difficulties which may attend this potentially fatal condition are highlighted by our experience with this family.Entities:
Mesh:
Year: 1993 PMID: 8487283 PMCID: PMC1016346 DOI: 10.1136/jmg.30.4.325
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318