Persistent Mullerian duct syndrome
Other Names for this Disease
- Female genital ducts in otherwise normal male
- Hernia uteri inguinale
- Persistent mullerian duct syndrome, types 1 and 2
- Persistent oviduct syndrome
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.
male reproductive organs and normal male external genitalia, but also have a uterus and fallopian tubes (female reproductive organs). The uterus and fallopian tubes develop from a structure called the Müllerian duct in the fetus, which normally breaks down in males. In males with PMDS, the Müllerian duct remains. Early signs of PMDS may include undescended testes (cryptorchidism) or inguinal hernias. The uterus and fallopian tubes are often noticed during surgery to treat these conditions. Other features of PMDS may include unusual or abnormal positioning of the testes and female reproductive organs; transverse testicular ectopia (when both testicles descend on the same side); and infertility. PMDS is caused by mutations in the AMH gene (PMDS type 1) or AMHR2 gene (PMDS type 2) and is inherited in an autosomal recessive manner. In some cases, the genetic cause is unknown. Treatment may involve surgery to place the testes within the scrotum and remove Müllerian structures.Persistent Müllerian duct syndrome (PMDS) is a disorder of sexual development that affects males. Affected males have normal
Last updated: 10/20/2015
- Persistent Müllerian duct syndrome. Genetics Home Reference. March, 2011; http://ghr.nlm.nih.gov/condition/persistent-mullerian-duct-syndrome.
- Jean-Yves Picard. Persistent Müllerian duct syndrome. Orphanet. January, 2009; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2856.
- Genetics Home Reference (GHR) contains information on Persistent Mullerian duct syndrome. This website is maintained by the National Library of Medicine.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Persistent Mullerian duct syndrome. Click on the link to view a sample search on this topic.