A Case of Familial Male-Limited Precocious Puberty with a Novel Mutation.

In this report, we present a case of FMPP with a novel mutation in the LHCGR gene, who has been responding well to therapy using both drugs. PMID: 32757547 [PubMed - as supplied by publisher]
Source: JCRPE Journal of Clinical Research in Pediatric Endocrinology - Category: Endocrinology Tags: J Clin Res Pediatr Endocrinol Source Type: research