| Literature DB >> 2918545 |
M Pembrey1, S J Fennell, J van den Berghe, M Fitchett, D Summers, L Butler, C Clarke, M Griffiths, E Thompson, M Super.
Abstract
The inheritance of Angelman's syndrome, a disorder characterised by mental retardation, epilepsy, ataxia, and a happy disposition, is debated because affected sibs occur less frequently than expected with autosomal recessive inheritance. After discovering two unrelated patients with a small deletion of the proximal long arm of chromosome 15, 10 further patients with Angelman's syndrome were reassessed. Five had apparently normal karyotypes, four had a deletion within 15q11-13, and one had a pericentric inversion, inv(15)(p11q13) involving the same chromosomal region. In the latter case, the healthy mother had the same pericentric inversion, indicating that the patient also had a submicroscopic mutation on his other chromosome 15. These data map the Angelman locus to 15q11-13 and suggest that de novo visible deletions (associated with a low recurrence risk) and autosomal recessively inherited cases combine to give an overall sib recurrence risk of less than 25%.Entities:
Mesh:
Year: 1989 PMID: 2918545 PMCID: PMC1015553 DOI: 10.1136/jmg.26.2.73
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318