Evaluation of 2407 fetuses in a Turkish population

CEYLANER G., CEYLANER S., Günyeli I., Ekici E., Celasun B., Danişman N.

Prenatal Diagnosis, cilt.27, sa.9, ss.800-807, 2007 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 27 Sayı: 9
  • Basım Tarihi: 2007
  • Doi Numarası: 10.1002/pd.1762
  • Dergi Adı: Prenatal Diagnosis
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.800-807
  • Anahtar Kelimeler: prenatal diagnosis, fetal diseases, abnormalities, autopsy, NEURAL-TUBE DEFECTS, FETAL ABNORMALITIES, CONGENITAL-MALFORMATIONS, TERMINATION, PREGNANCY, ANOMALIES, AUTOPSY, DEATH
  • Lokman Hekim Üniversitesi Adresli: Hayır

Özet

Objectives: Congenital anomalies and intrauterine fetal death (IUFD) are frequent problems in pregnancies. Detection of the etiology is important for genetic counseling, and presenting the geographic distribution of the causes of disorders is necessary for a national policy on precautions. Here, we report the findings of terminated fetuses due to IUFD and congenital anomalies in Turkish population. Methods: Physical examinations of fetuses and genetic evaluations of families were done. X-ray studies and autopsy were done in the event of necessity. Findings of these studies were combined with prenatal ultrasound results. All cases were classified according to ICD-10. Results: The number of fetuses examined was 2407. Out of these, 1268 fetuses had congenital anomalies. Neurologic anomalies and musculoskeletal system malformations were the most frequent disorders. Specific diagnoses were possible in 64% of all multiple malformation syndromes. Abnormal findings were detected in 18.8% of IUFD fetuses. Nine percent had congenital anomalies and 5.2% had cord complications. The percentage of twins and triplets was 7.5% and 13% of them had anomalies. Conclusion: Postmortem evaluation is useful to detect findings necessary for genetic counseling. Our protocol is effective especially in fetuses with congenital anomalies but it can detect only some of the fetal reasons in IUFD cases. A more detailed protocol is needed to investigate IUFD cases. Copyright © 2007 John Wiley & Sons, Ltd.