Sirenomelia (the Mermaid Syndrome): Report of Three Cases

被引:1
作者
Dicle, Nilgun [1 ]
Sayhan, Sevil [1 ]
Ayaz, Duygu [1 ]
Kececi, Sibel [1 ]
Sanci, Muzaffer [2 ]
机构
[1] Izmir Ege Obstet & Gynecol Educ & Res Hosp, Dept Pathol, Izmir, Turkey
[2] Izmir Ege Obstet & Gynecol Educ & Res Hosp, Dept Gynecol & Obstet, Izmir, Turkey
来源
TURKIYE KLINIKLERI TIP BILIMLERI DERGISI | 2010年 / 30卷 / 04期
关键词
Ectromelia; abnormalities;
D O I
10.5336/medsci.2008-8728
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sirenomelia is a rare and lethal malformation. It has been considered as an extreme form of caudal regression syndrome. This sporadic defect occurs in approximately I in 60000 newborn infants and has male predominance. Maternal diabetes mellitus is accepted to be an important predisposing factor and urogenital, gastrointestinal, cardiopulmonary and central nervous system defects are seen together with the anomaly. In this case presentation, we reported three cases of sirenomelia with multiple organ malformations. Variety of the associated anomalies and the pathological features of these rare cases may enlighten diagnosis of similar cases.
引用
收藏
页码:1392 / 1394
页数:3
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