Hypoprolactinemia as a Clue to Diagnosis of Mild Central Hypothyroidism due to IGSF1 Deficiency

Loss-of-function mutations of IGSF1 are an X-linked cause of central hypothyroidism (CeH) and hypoprolactinemia. A boy who is now 15.2 years old presented at the age of 7.69 years for evaluation of obesity. Previous thyroid function evaluation suggested CeH [FT4 0.6 ng/mL, thyroid-stimulating hormon...

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Detalles Bibliográficos
Autores principales: Papadimitriou, Anastasios, Papadopoulou, Anna, Kleanthous, Kleanthis, Papadimitriou, Dimitrios T., Papaevangelou, Vassiliki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291406/
https://www.ncbi.nlm.nih.gov/pubmed/31448769
http://dx.doi.org/10.4274/jcrpe.galenos.2019.2019.0085

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291406/
https://www.ncbi.nlm.nih.gov/pubmed/31448769
http://dx.doi.org/10.4274/jcrpe.galenos.2019.2019.0085

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