Journals / Medical Network Klinik Bilimler ve Doktor / 2001 / Cilt: 7 - Sayı: 6

Sirenomelia report of two case

Sirenomelia iki olgunun sunumu

Pages
854–856
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this article we discuss 2 cases which are not diagnosed ultrasonographically because of anhidroamnios and after the birth diagnosed as syrenomelia

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Sirenomelia is a disease, wich is seen one in 60,000 births and together with skeleton system anomalies, fusion in lower extremities, Urogenital defects, umblical arter abnormalities and congenital heart diseases.
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Key Findings & Data:It's known as marmeid syndrome.
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Conclusion & Impact:In this article we discuss 2 cases which are not diagnosed ultrasonographically because of anhidroamnios and after the birth diagnosed as syrenomelia
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Süt çocuğu · yenidoğan · hastalıklar

Abstract

Sirenomelia is a disease, wich is seen one in 60,000 births and together with skeleton system anomalies, fusion in lower extremities, Urogenital defects, umblical arter abnormalities and congenital heart diseases. It's known as marmeid syndrome. This disease is the lethal f arm of caudal regression syndrome. In this article we discuss 2 cases which are not diagnosed ultrasonographically because of anhidroamnios and after the birth diagnosed as syrenomelia

Özet

Sirenomelia 60,000 doğumda bir görülen; iskelet sistemi anomalileri alt extremitelerde füzyon, urogenital defektler, göbek arteri anomalileri kongenital kalp hastalıkları ile birlikte görülen bir hastalıktır. Deniz kızı sendromu olarak da bilinir. Kaudal regresyon sendromunun fatal seyreden ağır bir formudur. Bu yayında hastanemizde anhidroamnios nedeniyle ultrasonografik tanısı konamayan ancak doğumdan sonra sirenomelia tanısı alan iki olgu literatürler ışığında tartışıldı.

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Cite This Article

SANCI, M., GÜLER, A., MEYDAN, E., DİCLE, N., BAŞOĞUL, N., İSPAHİ, Ç. (2001). Sirenomelia report of two case. Medical Network Klinik Bilimler ve Doktor, Cilt: 7 - Sayı: 6, 854–856. https://ajindex.com/articles/278690

References (4)

  1. Jonathan S. WIGLEWORTH, Den B. SINGER. Textbook of fetal and perinatal Pathology, l.st. ed. Boston, Blackwell Scientific Publications, 1991; p:384. Sonek JD, Gabbe SG, London MB. Antenatal Diagnosis Sacral Agenezis Syndrome in a pregnancy complicated by diabetes mellitus. Am J Obstet Gynecol 1990; 162:806-811.
  2. Lenz W, Majer W. Congenital Malformations and Gestational diabetes. Lancet 1964; 2:1124-1126.
  3. Tannies P, Watesman D, Gellen J. Prenatal Diagnosis of Syrenomelia. Zentralbl Gynecol 1999; 95:121. Peter W. İn CALLEN. Obstetrics and gynecologic ultrasonography 1997; 314-317.
  4. Baxi L, Warren W, Collins MH,Timor Tritsch IE: Early detection of caudal regression syndrome with transvaginal scanning. Obst Gyn 1990; 75:486. Dardoni D, Freeman PC: Syrenomelia sequence. The Fetus 1991; 1:7553.