Williams syndrome: Autosomal dominant inheritance
- 15 September 1993
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 47 (4), 478-481
- https://doi.org/10.1002/ajmg.1320470409
Abstract
Williams syndrome (WS) usually occurs sporadically. Few familial cases of Williams syndrome have been described, and those reports have often lacked photographic documentation. We describe 3 families, including a 3-year-old boy and his 34-year-old father, a 2-year-old girl and her 30-year-old mother, and a 3-year-old girl and her 31-year-old mother. None of these patients has supravalvular aortic stenosis or chromosome abnormalities. In all 3 families, the parent with Williams syndrome was diagnosed after the identification of the syndrome in the affected child.Keywords
This publication has 17 references indexed in Scilit:
- Williams syndrome in twinsAmerican Journal of Medical Genetics, 2005
- Natural history of Williams syndrome: Physical characteristicsThe Journal of Pediatrics, 1988
- Williams syndrome.Journal of Medical Genetics, 1986
- Supravalvular aortic stenosis in a twin.Heart, 1978
- Familial occurrence of the Williams syndromeThe Journal of Pediatrics, 1977
- The Williams elfin facies syndromeThe Journal of Pediatrics, 1975
- Possible Dominant Inheritance of the Idiopathic Hypercalcemic SyndromeHuman Heredity, 1975
- Supravalvular aortic stenosis: Unusual observations in three patientsThe American Journal of Cardiology, 1969
- The spectrum of abnormalities in supravalvular aortic stenosisThe American Journal of Cardiology, 1967
- Supravalvular Aortic StenosisCirculation, 1961