A Rarely Seen Fetal Anomaly: Fraser Syndrome

Authors

  • Miğraci Tosun Department of Obstetrics and Gynecology and Faculty of Medicine Ondokuz Mayıs University, Samsun
  • Özlem Ulusoy Department of Obstetrics and Gynecology Sivas State Hospital, Sivas
  • Arif Kökcü Department of Obstetrics and Gynecology and Faculty of Medicine Ondokuz Mayıs University, Samsun
  • Mehmet Çetinkaya Department of Obstetrics and Gynecology and Faculty of Medicine Ondokuz Mayıs University, Samsun
  • Oğuz Aydın Department of Pediatric Genetics Faculty of Medicine Ondokuz Mayıs University, Samsun
  • Gönül Oğur Department of Pathology Faculty of Medicine Ondokuz Mayıs University, Samsun

Keywords:

Fetal anomaly, Fraser syndrome, Prenatal diagnosis

Abstract

There are about 200 published case reports of patients with Fraser syndrome and several comprehensive reviews have previously been published. Fraser syndrome has a recurrence risk of 25% among siblings, therefore prenatal diagnosis is an important task for the diagnostician counseling affected families. We aimed to report a case of Fraser Syndrome that was diagnosed prenatally at 19 weeks of gestation with multiple ultrasonographic anomalies and terminated at 21 weeks of gestation, to review prenatal diagnostic criteria and possible etiologic factors of Fraser syndrome.

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Published

2009-12-12

How to Cite

1.
Tosun M, Ulusoy Özlem, Kökcü A, Çetinkaya M, Aydın O, Oğur G. A Rarely Seen Fetal Anomaly: Fraser Syndrome. Gynecol Obstet Reprod Med [Internet]. 2009Dec.12 [cited 2021Jul.28];15(3):162-4. Available from: https://www.gorm.com.tr/index.php/GORM/article/view/395

Issue

Section

Case Reports

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