Prevalence estimation of Williams syndrome
- PMID: 12088082
- DOI: 10.1177/088307380201700406
Prevalence estimation of Williams syndrome
Abstract
There are limited population-based data on the occurrence of Williams syndrome. We estimated its prevalence combining data from two investigations. One was an epidemiologic study originally designed to assess the prevalence and etiology of mental retardation among 30,037 Norwegian children born between 1980 and 1985 and living in Akershus County on January 1, 1993. The other investigation was a national survey of Williams syndrome. In the first study, 213 children were referred for evaluation, whereas the second study comprised 57 cases with Williams syndrome born between 1970 and 1992, who were referred for evaluation from all Norwegian counties. The epidemiologic study revealed three children with Williams syndrome, whereas one additional case complying with our demographic criteria was identified in the national survey, thus giving a prevalence of 1 in 7500. In all cases, a typical chromosome 7q11.23 deletion was detected. We also conclude that Williams syndrome is not an uncommon cause of mental retardation, with a prevalence of approximately 6% of patients with genetic etiology.
Similar articles
-
[Williams syndrome: new insights into genetic etiology, pathogenesis and clinical aspects].Ned Tijdschr Geneeskd. 2001 Mar 3;145(9):396-400. Ned Tijdschr Geneeskd. 2001. PMID: 11253493 Review. Dutch.
-
A comparative study of hearing loss in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.J Pediatr. 2011 Feb;158(2):301-6. doi: 10.1016/j.jpeds.2010.07.056. Epub 2010 Sep 16. J Pediatr. 2011. PMID: 20846670
-
[Clinical aspects and genetics of Williams-Beuren syndrome. Clinical and molecular genetic study of 44 patients with suspected Williams-Beuren syndrome].Klin Padiatr. 2000 Nov-Dec;212(6):299-307. doi: 10.1055/s-2000-9605. Klin Padiatr. 2000. PMID: 11190824 German.
-
Williams syndrome in a preterm infant with phenotype of Alagille syndrome.Am J Med Genet A. 2008 Sep 15;146A(18):2407-11. doi: 10.1002/ajmg.a.32356. Am J Med Genet A. 2008. PMID: 18688871
-
Williams-Beuren syndrome: genes and mechanisms.Hum Mol Genet. 1999;8(10):1947-54. doi: 10.1093/hmg/8.10.1947. Hum Mol Genet. 1999. PMID: 10469848 Review.
Cited by
-
Synaptic plasticity and spatial working memory are impaired in the CD mouse model of Williams-Beuren syndrome.Mol Brain. 2016 Aug 2;9(1):76. doi: 10.1186/s13041-016-0258-7. Mol Brain. 2016. PMID: 27485321 Free PMC article.
-
Williams syndrome: reduced orienting to other's eyes in a hypersocial phenotype.J Autism Dev Disord. 2023 Jul;53(7):2786-2797. doi: 10.1007/s10803-022-05563-6. Epub 2022 Apr 20. J Autism Dev Disord. 2023. PMID: 35445369 Free PMC article.
-
Epigallocatechin-3-gallate improves cardiac hypertrophy and short-term memory deficits in a Williams-Beuren syndrome mouse model.PLoS One. 2018 Mar 19;13(3):e0194476. doi: 10.1371/journal.pone.0194476. eCollection 2018. PLoS One. 2018. PMID: 29554110 Free PMC article.
-
Attention to faces in Williams syndrome.J Autism Dev Disord. 2011 Sep;41(9):1228-39. doi: 10.1007/s10803-010-1141-5. J Autism Dev Disord. 2011. PMID: 21125323
-
Williams-Beuren syndrome shapes the gut microbiota metaproteome.Sci Rep. 2023 Nov 3;13(1):18963. doi: 10.1038/s41598-023-46052-9. Sci Rep. 2023. PMID: 37923896 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical