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familial male precocious puberty
Pathology:
- LH receptor is constitutively active
- constitutive secretion of testosterone by testicular Leydig cells
Genetics:
- activating mutation(s) of the LH receptor
- autosomal dominant inheritance
Clinical manifestations:
- isosexual precocious puberty in males
General
familial precocious puberty
Database Correlations
OMIM 176410
References
OMIM :accession 176410