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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2021
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| Materias: | |
| 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 |