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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Auteurs principaux:	Anastasios Papadimitriou, Anna Papadopoulou, Kleanthis Kleanthous, Dimitrios T. Papadimitriou, Vassiliki Papaevangelou
Format:	Artigo
Langue:	Inglês
Publié:	Pediatric Endocrinology and Diabetes Society 2020-06-01
Collection:	JCRPE
Sujets:	central hypothyroidism hypoprolactinemia igsf1
Accès en ligne:	http://www.jcrpe.org/archives/archive-detail/article-preview/hypoprolactinemia-as-a-clue-to-diagnosis-of-mild-c/30072
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