Clinical and genetic characteristics of boys with congenital hypogonadotropic hypogonadism: a single-center experience
CHH should be suspected in boys with micropenis and cryptorchidism. AMH and inhibin B are key markers for early detection of Leydig cell dysfunction, with genetic testing being essential for diagnosis.
Authors
- Dongxia Fu (ORCID: https://orcid.org/0000-0002-3591-4422)
- Xue Wu
- Jing Gao (ORCID: https://orcid.org/0000-0001-8797-9933)
- Huizhen Wang (ORCID: https://orcid.org/0000-0001-5588-5545)
- Haiyan Wei (ORCID: https://orcid.org/0000-0003-1044-6594)
- Yongxing Chen (ORCID: https://orcid.org/0000-0002-4131-137X)
Institutions
- Zhengzhou Children's Hospital (CN)
Publication Details
- Journal
- BMC Pediatrics
- Published
- 2025-11-25
- DOI
- https://doi.org/10.1186/s12887-025-06162-x
- Primary Topic
- Hypothalamic control of reproductive hormones
- Type
- article
- Field-Weighted Citation Impact
- 0.00