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Scholars Journal of Medical Case Reports | Volume-5 | Issue-12
Williams-Beuren Syndrome: About A Case
Sara Askaoui, Guizlane El Mghari, Nawal El Ansari
Published: Dec. 30, 2017 | 133 148
DOI: 10.36347/sjmcr.2017.v05i12.009
Pages: 841-843
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Abstract
Williams-Beuren syndrome is a rare genetic disease with an incidence of 1 / 200000, characterized by evocative facial dysmorphism, cardiac malformations, psycho-motor retardation, specific cognitive and behavioral profile and impairment endocrine. Its treatment is symptomatic so that its management is multidisciplinary. We report a case of Williams-Beuren syndrome revealed by stunting.