Mullerian dysgenesis

Academic Article


  • The multifaceted syndrome of mullerian dysgenesis appears to represent a defect in mesodermal organization and is often associated with renal and skeletal anomalies. This report discusses the embryology, multifactorial etiology, clinical presentation and management of the syndrome from a historical standpoint and details our experience with 35 affected patients. Both Frank dilatation and McIndoe vaginoplasty appear to be acceptable means of therapy. The therapeutic success depends to a large extent on the psychosocial adaptation of the patient.
  • Published In

    Author List

  • Varner RE; Younger JB; Blackwell RE
  • Start Page

  • 443
  • End Page

  • 450
  • Volume

  • 30
  • Issue

  • 6