Partial Thyroid Hormone-Binding Globulin Deficiency: A Case Report and Literature Review

BACKGROUND: Thyroxine binding globulin (TBG) deficiency is a rare thyroid disease, mostly caused by genetic mutations and acquired by X-linked recessive inheritance. The clinical features of children with TBG deficiency and their family members were summarised and the Serpina7 gene mutation was anal...

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Detalles Bibliográficos
Autores principales: Liu, Xuefang, Li, Suyan, Xiong, Jingni, Chen, Dandan, Jiang, Chan, Zeng, Liankun, Qiu, Youyan, Xia, Bi-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387242/
https://www.ncbi.nlm.nih.gov/pubmed/37525823
http://dx.doi.org/10.2147/DMSO.S413048

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387242/
https://www.ncbi.nlm.nih.gov/pubmed/37525823
http://dx.doi.org/10.2147/DMSO.S413048

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