Challenges in clinical diagnosis of williams-beuren syndrome in sub-saharan africans: case reports from cameroon.

ABSTRACT: Williams-Beuren syndrome (WBS) is a rare neurodevelopmental condition caused by a recurrent chromosomal microdeletion involving about 28 contiguous genes at 7q11.23. Most patients display a specific congenital heart defect, characteristic facial features, a particular behavior, and intellectual disability. Cases from sub-Saharan Africa have been seldom reported. The present study describes 3 Cameroonian patients affected by WBS, aged 19 months, 13 and 14 years, in whom the diagnosis was confirmed by fluorescent in situ hybridization (FISH) and comparative genomic hybridization (CGH). The first patient presented with a congenital heart defect, the second and third with learning difficulties as well as developmental and behavioral issues. In the latter 2 cases, the facial phenotypes were sim

SUBMITTER: Tekendo-Ngongang C 

PROVIDER: S-EPMC4281575 | biostudies-literature | 2014 Dec

REPOSITORIES: biostudies-literature