American Journal of Medical Genetics · 1993 · 167 citations · 16 references
Life SciencesGeneticsPediatricsHuman GeneticsMedical GeneticsPediatric GeneticsChromosomal AbnormalitiesCongenital DisordersCongenital Heart DiseaseGenetic DisordersGenetic SyndromesMendelian DisordersConstitutional Chromosome AbnormalitiesCytogenetic AbnormalitiesFamilial Congenital Heart DiseaseFamilial SyndromesInherited Disorder PedigreesParental Chromosomal AbnormalitiesWilliams Syndrome
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.
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J. C. P. Williams, Brian G. Barratt‐Boyes, J. B. Lowe · Circulation · 1961 · 1.1K citations · Full text
Medicine, Cardiology, Surgery +8
Natural history of Williams syndrome: Physical characteristics
Colleen A. Morris, Susan A. Demsey, Claire O. Leonard et al. · The Journal of Pediatrics · 1988 · 676 citations
The Williams elfin facies syndrome
Kenneth Lyons Jones, David W. Smith · The Journal of Pediatrics · 1975 · 241 citations
The Williams syndrome: objective definition and diagnosis
M. Preus · Clinical Genetics · 1984 · 146 citations
Colleen A. Morris, Claire O. Leonard, Constance Dilts et al. · American Journal of Medical Genetics · 2005 · 134 citations
Medicine, Cardiology, Urology +12