Prenatal diagnosis of fetal gallbladder duplication associated with uncommon chromosomal anomaly (46, XX, t(X; 10) (p11.2;q24.3) [20])


COMERT E. H. , ŞAL H. , KART C. , GUVEN E. S. G. , GÜVEN S.

CLINICAL AND EXPERIMENTAL OBSTETRICS & GYNECOLOGY, cilt.46, ss.980-981, 2019 (SCI İndekslerine Giren Dergi) identifier

  • Cilt numarası: 46 Konu: 6
  • Basım Tarihi: 2019
  • Doi Numarası: 10.12891/ceog4757.2019
  • Dergi Adı: CLINICAL AND EXPERIMENTAL OBSTETRICS & GYNECOLOGY
  • Sayfa Sayısı: ss.980-981

Özet

Fetal gallbladder duplication is a rare congenital malformation. In the literature only a few cases of fetal gallbladder duplication in utero is reported. A 22-year-old woman was referred to this hospital at 26 weeks of gestation for a routine ultrasound examination. A fetal duplication of gallbladder accompanied was diagnosed with ultrasonography (axial section of fetal abdomen on sonography showed two hypoechoic cyst-like structures). The diagnosis of duplication of gallbladder, was also confirmed with MM. The result of cordo-centesis was reported as 46, XY, t(X;10) (p11.2;q24.3) [201. Antenatal/natal/postnatal care was unremarkable. A novel chromosomal mutation (46, XX, t(X;10) (p11.2;q24.3) [20]) with duplicated fetal gallbladder which has not been reported previously was described.