| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5691803 | European Journal of Obstetrics & Gynecology and Reproductive Biology | 2016 | 5 Pages |
Abstract
Our study confirms complexity and clinical heterogeneity of MRKHS. Concomitant congenital malformations are present in about half of MRKHS women. A significant proportion of patients have coexisting anomalies of at least two organ systems. The most common coexisting findings are musculoskeletal and renal abnormalities. Chromosomal aberrations may be present in patients with either typical or atypical form of MRKHS.
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Authors
Karina Kapczuk, Kinga Iwaniec, Zbigniew Friebe, Witold KÄdzia,