Sirenomelia (mermaid syndrome): A rare anomaly
نویسندگان
چکیده
منابع مشابه
Sirenomelia: the Mermaid Syndrome
Sirenomelia (the Mermaid Syndrome) is a rare and lethal congenital anomaly with an incidence of one in 100,000 of normal pregnancies. It is an extremely rare set of birth defects, which can vary in expression. The condition gets its name from one of the defects present, which is a fusing of the legs. The fused nature of the legs has been compared to a mermaid in appearance, hence the name. The ...
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Sirenomelia is an uncommon congenital malformation. We describe a newborn with clinical features of sirenomelia with fused lower limbs, anal atresia, bilateral renal agenesis and a single umbilical artery.
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This case involves the rare congenital disorder Sirenomelia, a diagnosis initially suspected during prenatal ultrasound and later confirmed by prenatal MRI. Sirenomelia, or mermaid syndrome, is mainly characterized by variable fusion of the lower limbs and by genitourinary anomalies. The vast majority of cases of this disease result in death secondary to associated renal agenesis or hypoplasia....
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caudal regression syndrome (caudal dysplasia sequence) is a rare congenital malformation. it has a spectrum ranging from simple anal atresia to the absence of sacral, lumbar and possibly lower thoracic vertebrae and the most severe form called sirenomelia (mermaid syndrome). sirenomelia has a sole characteristic, which is the limbs fusion, with multiple internal structural abnormalities particu...
متن کاملmermaid syndrome, sirenomelia: a case report and review of literature
abstract sirenomelia is a rare anomaly of caudal region of the body presented with fusion of lower limbs in which genito-urinary, gastrointestinal, cardiovascular and neural tube anomalies are found in most cases. we introduce a case of severe oligohydramnios, which had characteristic aspects of sirenomelia at the time of delivery and review the pertinent articles. all in all it is our aim to p...
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ژورنال
عنوان ژورنال: African Journal of Paediatric Surgery
سال: 2008
ISSN: 0189-6725
DOI: 10.4103/0189-6725.44190