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Arterial Hypertension in a Child with Williams-Beuren Syndrome (7q11.23 Chromosomal Deletion)

We report the case of a 7-year-old male child diagnosed with Williams-Beuren syndrome and arterial hypertension refractory to clinical treatment. The diagnosis was confirmed by genetic study. Narrowing of the descending aorta and stenosis of the renal arteries were also diagnosed. Systemic vascular...

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Bibliographic Details
Published in:Arquivos brasileiros de cardiologia 2002-08, Vol.79 (2), p.177-180
Main Authors: Sylos, Cristina de, Pereira, Alexandre C., Azeka, Estela, Miura, Nana, Mesquita, SĂ´nia Maria Ferreira, Ebaid, Munir
Format: Article
Language:English
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Summary:We report the case of a 7-year-old male child diagnosed with Williams-Beuren syndrome and arterial hypertension refractory to clinical treatment. The diagnosis was confirmed by genetic study. Narrowing of the descending aorta and stenosis of the renal arteries were also diagnosed. Systemic vascular alterations caused by deletion of the elastin gene may occur early in individuals with Williams-Beuren syndrome, leading to the clinical manifestation of systemic arterial hypertension refractory to drug treatment.
ISSN:0066-782X
1678-4170
1678-4170
DOI:10.1590/S0066-782X2002001100009