نتایج جستجو برای: mermaid syndrome

تعداد نتایج: 622042  

Journal: :Sri Lanka Journal of Obstetrics and Gynaecology 2014

Journal: :Journal of Natural Science, Biology and Medicine 2015

Journal: :Journal of prenatal medicine 2009
Alessandro Cavaliere Angela Dinatale Giovanna Cardinale Santina Ermito Tindara La Galia Barbara Circosta Laura Imbruglia Giusi Rapisarda

OBJECTIVE Sirenomelia (Mermaid syndrome) is a rare anomaly of caudal region of the body, presented with fusion of the lower limbs. Genito-urinary, gastro-intestinal, neural tube and vertebral anomalies are found in most cases. METHODS We present a case of sirenomelia diagnosed in the first tri-mester, associated with dextrocardia, and omphalocele CONCLUSION First trimester diagnosis of sire...

Journal: :JPMA. The Journal of the Pakistan Medical Association 2009
Rozina Sikandar Shama Munim

Sirenomelia, the Mermaid Syndrome is a rare and lethal congenital anomaly with an incidence of one in 60,000 to 70,000 pregnancies. Sirenomelia is characterized by complete fusion of the lower limbs, commonly associated with renal agenesis, absent external genitalia and other gastrointestinal defects. Another pathognomonic finding is the presence of single umbilical, persistent vitelline artery...

Journal: :Ellipsis: A Journal of Art, Ideas, and Literature 2014

2016
Anupama Praveen Gupta Sanjay Nanaji Parate Dinkar T. Kumbhalkar

We report a case of sirenomelia baby (mermaid syndrome) born to a thirty years old female at 36 weeks of gestation. It is a rare syndrome in which there is fusion of lower limbs. Classification of caudal regression syndrome (CRS) from sirenomelia is still debated. According to some authors, this syndrome should be classified separately from caudal regression syndrome and is likely to be the res...

2012
K Ramesh Reddy S Srinivas Shiva Kumar Surweshwar Reddy Hari Prasad G M Irfan

We are presenting two cases of Sirenomelia (Mermaid Syndrome), which is an extreme example of the caudal regression syndrome. It invariably presents with lower limb fusion, sacral and pelvic bony anomalies, absent external genitalia, imperforate anus, and renal agenesis or dysgenesis. There are approximately 300 cases reported in the literature, 15% of which are associated with twinning, most o...

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