| Literature DB >> 8030674 |
W H Linssen1, M J Van den Bent, H G Brunner, P J Poels.
Abstract
We report on 3 sibs (2 males and one female) with sensorineural deafness. The presence of ovarian dysgenesis in the girl suggested a diagnosis of Perrault syndrome. In addition our patients have a sensory polyneuropathy and amelogenesis imperfecta. Two of the patients have mild mental retardation, fine choreatic movements, and dyspraxia. It is discussed whether these findings are part of a separate clinical entity or should be included within the spectrum of the Perrault syndrome.Entities:
Mesh:
Year: 1994 PMID: 8030674 DOI: 10.1002/ajmg.1320510117
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299