A bibliometric analysis of Kallmann syndrome: trends, hotspots, and future directions
Abstract Background Kallmann syndrome (KS) is a rare congenital disorder characterized by hypogonadotropic hypogonadism secondary to deficient gonadotropin-releasing hormone (GnRH) secretion, often accompanied by partial or complete anosmia. Deficient GnRH secretion results in decreased levels of fo...
Furkejuvvon:
| Váldodahkkit: | , , , , , , |
|---|---|
| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
BMC
2026-05-01
|
| Ráidu: | Orphanet Journal of Rare Diseases |
| Fáttát: | |
| Liŋkkat: | https://doi.org/10.1186/s13023-026-04378-3 |
| Fáddágilkorat: |
Eai fáddágilkorat, Lasit vuosttaš fáddágilkora!
|