Alström syndrome with a novel mutation of ALMS1 and Graves’ hyperthyroidism: A case report and review of the literature

BACKGROUND: Alström syndrome (AS, OMIM ID 203800) is a rare disease involving multiple organs in children and is mostly reported in non-Chinese patients. In the Chinese population, there are few reports on the clinical manifestations and pathogenesis of AS. This is the first report on the associatio...

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Detalles Bibliográficos
Autores principales: Zhang, Juan-Juan, Wang, Jun-Qi, Sun, Man-Qing, Xu, De, Xiao, Yuan, Lu, Wen-Li, Dong, Zhi-Ya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080750/
https://www.ncbi.nlm.nih.gov/pubmed/33969109
http://dx.doi.org/10.12998/wjcc.v9.i13.3200

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080750/
https://www.ncbi.nlm.nih.gov/pubmed/33969109
http://dx.doi.org/10.12998/wjcc.v9.i13.3200

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