Dizygotic twin sisters with normosmic idiopathic hypogonadotropic hypogonadism caused by an gene variant

Isolated hypogonadotropic hypogonadism (IHH) is a rare genetic disorder that is clinically and genetically heterogeneous. It is characterized by absent or incomplete pubertal development owing to an isolated defect in the production, secretion, or action of gonadotropin-releasing hormone. The incide...

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Main Authors: Jaewon Choe (Author), Jae Hyun Kim (Author), Young Ah Kim (Author), Jieun Lee (Author)
Formato: Livro
Publicado em: Korean Society of Pediatric Endocrinology, 2020-07-01T00:00:00Z.
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