Familial male-limited precocious puberty due to an activating mutation of the LHCGR: a case report and literature review
Familial male-limited precocious puberty (FMPP) is a rare form of gonadotropin-independent precocious puberty that is caused by an activating mutation of the LHCGR gene. Herein, we report a case of FMPP with a mutation of the LHCGR gene in a Korean boy with familial history of precocious puberty thr...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
Korean Society of Pediatric Endocrinology,
2024-02-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |