Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter→q22:)

AYDOS, OYA; Tükün, A.; Bökesoy, I.

doi:10.1007/s00404-001-0274-3

Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter→q22:)

AYDOS O. S., Tükün A., Bökesoy I.

Archives of Gynecology and Obstetrics, cilt.267, sa.3, ss.173-174, 2003 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 267 Sayı: 3
Basım Tarihi: 2003
Doi Numarası: 10.1007/s00404-001-0274-3
Dergi Adı: Archives of Gynecology and Obstetrics
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.173-174
Anahtar Kelimeler: Fluorescein in situ hybridization, Gonadal dysgenesis, Mayer-Rokitansky-Kuster-Hauser syndrome, Xq deletion
Ankara Üniversitesi Adresli: Evet

Özet

The association of mullerien duct with gonadal dysgenesis is extremely rare. We report such a case in a 19 year-old white woman with a 46,X,del(X)(pter→q22:) karyotype.