Multiple bladder diverticula with Williams-Beuren syndrome: a case report

Williams-Beuren syndrome (WBS) is an autosomal dominant disorder caused by a gene deletion on chromosome 7q11.23. Patients with WBS usually show a group of features such as developmental delay, cardiovascular anomalies, mental retardation, and characteristic facial appearance. It occurs in 1:7,500 l...

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Detalles Bibliográficos
Autores principales: Chen, Jing, Mao, Jianhua, Ye, Lezhen, Zong, Dongmei, Qiao, Xiaohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804474/
https://www.ncbi.nlm.nih.gov/pubmed/33457309
http://dx.doi.org/10.21037/tp-20-311

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804474/
https://www.ncbi.nlm.nih.gov/pubmed/33457309
http://dx.doi.org/10.21037/tp-20-311

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