Treatment of congenital hypogonadotropic hypogonadism in male patients
Congenital hypogonadotropic hypogonadism (CHH) is characterized by complete or partial failure of pubertal development because of inadequate secretion of gonadotropic hormones. CHH consists of hypogonadotropic hypogonadism with anosmia or hyposmia, Kallmann syndrome, and the normosmic variation norm...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Korean Society of Pediatric Endocrinology,
2022-09-01T00:00:00Z.
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