Molecular genetics of isolated hypogonadotropic hypogonadism and Kallmann syndrome.
作者： Beate Karges , Nicolas de Roux
DOI: 10.1159/000084094
关键词: Internal medicine 、 Endocrinology 、 Molecular genetics 、 Luteinizing hormone 、 Kallmann syndrome 、 Medicine 、 Isolated hypogonadotropic hypogonadism 、 Partial failure
摘要: Isolated hypogonadotropic hypogonadism (IHH) is characterized by complete or partial failure of pubertal development due to impaired secretion luteinizing hormone (LH) and follicle-stimulating ho
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