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J Pediatr ; 179: 263-265, 2016 12.
Article in English | MEDLINE | ID: mdl-27640350

ABSTRACT

Ten girls with sporadic central precocious puberty were screened for mutations in the maternally imprinted gene MKRN3. We detected 1 novel frameshift mutation (p.Arg351Serfs*44) and a previously described mutation (p.Pro161Argfs*10). In the course of investigating the family, genetic analysis found 2 asymptomatic males with paternally inherited MKRN3 mutations, which has not been reported in previous studies.


Subject(s)
Asymptomatic Diseases , Mutation , Paternal Inheritance , Puberty, Precocious/genetics , Ribonucleoproteins/genetics , Child , Child, Preschool , Female , Humans , Male , Pedigree , Ubiquitin-Protein Ligases
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