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Males with Paternally Inherited MKRN3 Mutations May Be Asymptomatic
Mihaela S Dimitrova-Mladenova1, Elisaveta M Stefanova1, Maria Glushkova2
1Department of Endocrinology and Genetics, University Children's Hospital, Medical University Sofia, Sofia, Bulgaria.
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.
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