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Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome: A historical perspective

2014; Elsevier BV; Volume: 555; Issue: 1 Linguagem: Inglês

10.1016/j.gene.2014.09.045

1879-0038

Sourav S. Patnaik, Bryn Brazile, Vani Dandolu, Peter L. Ryan, Jun Liao,

Female Genital Mutilation/Cutting Issues

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital defect of the Müllerian ducts characterized by uterovaginal agenesis and underdeveloped female genital organs. This paper is a tribute to the contributors of this condition - August Franz Joseph Karl Mayer, Karl Freiherr von Rokitansky, Hermann Küster and Georges André Hauser. In addition to their contributions, we have discussed findings and reports of similar defects from other important scientists (Hippocrates, Albucasis, etc.) dating as far back as 460B.C. We have also discussed the disease types and different classification systems including VCUAM and AFS/ASRM among others. Even with several surgical and non-surgical treatment options, there are still many questions that remain unanswered and very little is known about the etiology or genetic predisposition of this condition.