Premature centromeric divisions and prominent telomeres in a patient with persistent Mullerian duct syndrome
- 28 June 2008
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 37 (1) , 69-73
- https://doi.org/10.1111/j.1399-0004.1990.tb03393.x
Abstract
A 35-year-old, rare male pseudohermaphrodite with inguinal hernia, testis, fallopian tube and uterus, symptoms referrable to persistent Mullerian duct syndrome, is described. The patient has a 46,XY karyotype in 50% of metaphases, while the remaining metaphases show premature cnetromeric divisions and hypoploid counts.Keywords
This publication has 3 references indexed in Scilit:
- Premature centromere division dominantly inherited in a subfertile familyCytogenetic and Genome Research, 1986
- Familial Persistent Müllerian Duct SyndromeJournal of Urology, 1976
- Pseudovaginal perineoscrotal hypospadiasClinical Genetics, 1972