Atatürk Üniversitesi Atatürk Üniversitesi
Ara
Yayınlara dön
Makale Tam Makale Uluslararası 2012

A case of sirenomelia sequence

Mevlit Ikbal, Hasan Kahveci, Basak Adakli Aksoy, Fuat Laloğlu, Ebru Kacmaz, Muhammed Yunus Alp

PAKISTAN JOURNAL OF MEDICAL SCIENCES Cilt 28 · Sayı 5 · ss. 968–970 · 01.10.2012

Özet

Sirenomelia sequence is a rare congenital anomaly. This is also known as "mermaid syndrome" because of typical feature of lower limb. Sirenomelia sequence is characterized with a single midline lower limb. Our case was an infant delivered at 34 gestational weeks by spontaneous vaginal delivery from a 34 years old gravida 2, para 0. Parents are not relative. Infant has one femur, one tibia and one phalanx at lower extremity. Calcaneus, metatarsals and other bones of the foot are absent. Patient has anal atresia and renal agenesy. Determination of sex was impossible since external genitalia was absent. Although some risk factors (e. g. maternal diabetes) have been suggested, etiolgy of sirenomelia sequence is debated. In this report, we describe a premature infant with sirenomelia sequence because of very rare presentation.

Anahtar kelimeler

Sirenomelia sequence Congenital abnormalities

Atıf için künye

Ikbal, M., Kahveci, H., Aksoy, B. A., Laloğlu, F., Kacmaz, E., & Alp, M. Y. (2012). A case of sirenomelia sequence. PAKISTAN JOURNAL OF MEDICAL SCIENCES, 28(5), 968–970.

BibTeX
@article{ikbal2012-222506,
  author = {Ikbal, Mevlit and Kahveci, Hasan and Aksoy, Basak Adakli and Laloğlu, Fuat and Kacmaz, Ebru and Alp, Muhammed Yunus},
  title = {A case of sirenomelia sequence},
  journal = {PAKISTAN JOURNAL OF MEDICAL SCIENCES},
  year = {2012},
  volume = {28},
  number = {5},
  pages = {968--970},
  issn = {1682-024X},
  url = {https://akademik.atauni.edu.tr/yayinlar/222506-a-case-of-sirenomelia-sequence}
}