A case report of Williams syndrome with main clinical manifestation of hypercalcemia and gastrointestinal bleeding as the main clinical manifestations, and with an accompanying literature review

BACKGROUND: Williams syndrome is an autosomal dominant multisystem disorder caused by a 1.5–1.8 Mb deletion on chromosome 7q11.23. It is characterized by facial deformations, cardiovascular abnormalities, developmental delays, gastrointestinal manifestations, and endocrine disorders. CASE DESCRIPTIO...

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Detalles Bibliográficos
Autores principales: Meng, Hong, Jia, Yue‐Xin, Yang, Hui‐Min, Gao, Xin, Li, Cha‐Gan‐Hu, Xin, Guo‐Yan, Wang, Yu‐Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Brief Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454276/
https://www.ncbi.nlm.nih.gov/pubmed/37337730
http://dx.doi.org/10.1002/brb3.3131

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