نتایج جستجو برای: sirenomelia

تعداد نتایج: 381  

2014
Swagat Mahapatra Suruchi Ambasta

Introduction: Sirenomelia is a congenital structural anomaly characterized by abnormal development of the caudal region of the body with varying degrees of fusion of lower limbs. Most of the times, the condition is fatal for the baby. Most babies do not survive even after surgery. Fifty percent of cases are seen as stillbirths, and it is much more common in identical twins. This abnormality was...

2010
Anis Fadhlaoui Mohamed Khrouf Soumaya Gaigi Fethi Zhioua Anis Chaker

We report a case of sirenomelia sequence observed in an incident of preterm labor during the 29th gestational week. According to some authors, this syndrome should be classified separately from caudal regression syndrome and is likely to be the result of an abnormality taking place during the fourth gestational week, causing developmental abnormalities in the lower extremities, pelvis, genitali...

طائی, نادره , طرهانی, فریبا , مهرزاد صفدری, علی ,

Sirenomelia is a very rare anomaly with incidence rate of one in every 100000 births .With fused legs and other different anomalies that can't be alive more than few days after birth. Etiology of Sirenomelia is unknown , Maternal diabetes mellitus and embryonic exposure with teratogenic agents have been proposed as possible causative factors . We report a case of sir...

Journal: :Journal of medical genetics 1997
C P Chen S L Shih F F Liu S W Jan

Cebocephaly and sirenomelia are uncommon birth defects. Their association is extremely rare; however, the presence of spina bifida with both conditions is not unexpected. We report on a female still-birth with cebocephaly, alobar holoprosencephaly, cleft palate, lumbar spina bifida, sirenomelia, a single umbilical artery, and a 46,XX karyotype, but without maternal diabetes mellitus. Our case a...

2012
Charles Upshaw Manohar Roda Majid Khan

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....

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...

Journal: :Journal of medical genetics 1992
B Källén E E Castilla P A Lancaster O Mutchinick L B Knudsen M L Martínez-Frías P Mastroiacovo E Robert

Infants with cyclopia or sirenomelia are born at an approximate rate of 1 in 100,000 births. Eight malformation monitoring systems around the world jointly studied the epidemiology of these rare malformations: 102 infants with cyclopia, 96 with sirenomelia, and one with both conditions were identified among nearly 10.1 million births. Maternal age is somewhat increased for cyclopia, indicating ...

Journal: :Indian Journal of Pathology and Microbiology 2009

2012
Frederick LI Morfaw Philip N Nana John Svigos Frederick Morfaw Laxmi Baxi

Sirenomelia is a rare congenital malformative disorder characterized by fusion of the lower limbs giving a characteristic mermaid-like appearance to the affected foetus. We report a case of sirenomelia occurring in a 19 year old Cameroonian woman following premature rupture of membranes and associated cord prolapse. This is the first documented case in this country. We highlight some of the cul...

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...

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