| Autor: |
Bousfiha N; Department of Gynecology Obstetric I, Teaching Hospital Hassan II, Fez 30000, Morocco., Errarhay S, Saadi H, Ouldim K, Bouchikhi C, Banani A |
| Jazyk: |
angličtina |
| Zdroj: |
Obstetrics and gynecology international [Obstet Gynecol Int] 2010; Vol. 2010, pp. 847370. Date of Electronic Publication: 2010 Dec 29. |
| DOI: |
10.1155/2010/847370 |
| Abstrakt: |
Introduction. The association of gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome is very rare and appears to be coincidental, independent of chromosomal anomalies. Case Report. We report the case of a 19-year-old woman who presented primary amenorrhea and impuberism. The endocrine study revealed hypergonadotrophic hypogonadism. The karyotype was normal, 46XX. No chromosome Y was detected at the FISH analysis. Internal genitalia could not be identified on the pelvic ultrasound and pelvic MRI. Laparoscopy was undertaken and revealed concomitant ovarian dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome. There were no other morphological malformations. Conclusion. The pathogenesis of the association of gonadal dysgenesis and Mayer Rokitansky kuster hauser syndrome is still mysterious. The treatment is based essentially on hormone substitution therapy. The fertility prognosis is unfortunately compromised. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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