Persistent Mullerian duct syndrome

An autosomal recessive congenital abnormality where mullerian derivatives, uterus and tubes, persist in otherwise normally virilized males. Mutations in the AMH gene and AMHR2 gene have been identified. OMIM: 261550

Also Known As:

Hernia uteri inguinale; Persistent Muellerian duct syndrome; Persistent Mullerian Duct Syndrome, Types I And II; Persistent Müllerian Duct Syndrome; Persistent mullerian duct syndrome, types 1 and 2; Persistent oviduct syndrome; Pseudohermaphroditism, male internal

Urogenital Diseases: 126
- Urogenital Abnormalities: 76
  - Disorders of Sex Development: 730
    - 46,XY Disorder of Sex Development: 472
      - Persistent Mullerian duct syndrome: 81
- Female Urogenital Diseases and Pregnancy Complications
  - Female Urogenital Diseases
    - Urogenital Abnormalities: 76
      - Disorders of Sex Development: 730
        46,XY Disorder of Sex Development: 472
        Persistent Mullerian duct syndrome: 81
- Male Urogenital Diseases
  - Urogenital Abnormalities: 76
    - Disorders of Sex Development: 730
      - 46,XY Disorder of Sex Development: 472
        Persistent Mullerian duct syndrome: 81
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Urogenital Abnormalities: 76
    - Disorders of Sex Development: 730
      - 46,XY Disorder of Sex Development: 472
        Persistent Mullerian duct syndrome: 81
Endocrine System Diseases: 968
- Gonadal Disorders: 30
  - Disorders of Sex Development: 730
    - 46,XY Disorder of Sex Development: 472
      - Persistent Mullerian duct syndrome: 81

Sabri Cansaran Selected Research

Sabri Cansaran Research Topics

Disease

Therapy/Procedure