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

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Atıf İçin Kopyala

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

CLINICAL AND EXPERIMENTAL OBSTETRICS & GYNECOLOGY, cilt.46, sa.6, ss.980-981, 2019 (SCI-Expanded)

• Yayın Türü: Makale / Tam Makale
• Cilt numarası: 46 Sayı: 6
• Basım Tarihi: 2019
• Doi Numarası: 10.12891/ceog4757.2019
• Dergi Adı: CLINICAL AND EXPERIMENTAL OBSTETRICS & GYNECOLOGY
• Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Sayfa Sayıları: ss.980-981
• Karadeniz Teknik Üniversitesi Adresli: Evet

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.