Congenital hypopituitarism due to novel compound heterozygous POU1F1 gene mutation: A case report and review of the literature

Failure to thrive is one of the most common complaints in the endocrinology and genetics clinic. An 8-month-old girl with presentation of motor developmental delay, failure to thrive, and midline facial defects, with history of hypoglycemia at birth and central congenital hypothyroidism (CCH), was b...

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Detalles Bibliográficos
Autores principales: Chen, Wei-Yu, Niu, Dau-Ming, Chen, Li-Zhen, Yang, Chia-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593650/
https://www.ncbi.nlm.nih.gov/pubmed/34815942
http://dx.doi.org/10.1016/j.ymgmr.2021.100819

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593650/
https://www.ncbi.nlm.nih.gov/pubmed/34815942
http://dx.doi.org/10.1016/j.ymgmr.2021.100819

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