Congenital isolated GnRH, LH, or FSH deficiency can cause secondary hypogonadism, including conditions such as Kallmann’s syndrome, Prader-Willi syndrome, Lawrence-Moon syndrome, GnRH receptor mutations, beta-subunit mutations in LH or FSH, or kisspeptin/G protein-coupled receptor fifty-four mutations.

Authors

• Person: Not available Organization: National Library of Medicine
  Physiology, Male Reproductive System - StatPearls - NCBI Bookshelf

Sources

• Physiology, Male Reproductive System - StatPearls - NCBI Bookshelf www.ncbi.nlm.nih.gov National Library of Medicine via serper

Referenced by nodes (3)

• luteinizing hormone (LH) concept
• FSH concept
• Gonadotropin-releasing hormone concept