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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| Principais autores: | , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Pediatric Endocrinology and Diabetes Society
2020-06-01
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| Serier: | JCRPE |
| Fag: | |
| Online adgang: |
http://www.jcrpe.org/archives/archive-detail/article-preview/hypoprolactinemia-as-a-clue-to-diagnosis-of-mild-c/30072
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