Simpson−Golabi−Behmel syndrome type 1 with subclinical hypothyroidism: A case report

RATIONALE: Simpson−Golabi−Behmel syndrome type 1 (SGBS1) is caused by mutations in GPC3 or in both GPC3 and GPC4. Physical manifestations of SGBS1 include fetal overgrowth and macrostomia, macroglossia. Subclinical hypothyroidism has never been reported in SGBS1 cases. PATIENT CONCERNS: An 8-days-ol...

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Detalles Bibliográficos
Autores principales: Zhang, Jing, Mu, Kai, Xu, Haiyan, Guo, Yuehua, Liu, Zhijie, Wang, Liling, Li, Jiahui, Zhang, Fengjuan, Kou, Yan, Yuan, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
6200
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824639/
https://www.ncbi.nlm.nih.gov/pubmed/31651874
http://dx.doi.org/10.1097/MD.0000000000017616

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824639/
https://www.ncbi.nlm.nih.gov/pubmed/31651874
http://dx.doi.org/10.1097/MD.0000000000017616

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