| Literature DB >> 2805105 |
A Gerinec, B Spissáková, M Chynoranský.
Abstract
The authors discuss a rare case, unique in our literature, of the familial incidence of Hallermann-Streiff's syndrome and the treatment of some of its complications. Special emphasis is laid on genetic analysis which provides evidence of autosomal dominant heredity with a variable expressivity of the pathological gene, and which must be applied in genetic consultations.Entities:
Mesh:
Year: 1989 PMID: 2805105
Source DB: PubMed Journal: Cesk Oftalmol ISSN: 0009-059X