نتایج جستجو برای: sirenomelia

تعداد نتایج: 381  

2012
Kentaro Suzuki Yasuha Adachi Tomokazu Numata Shoko Nakada Motoko Yanagita Naomi Nakagata Sylvia M. Evans Daniel Graf Aris Economides Ryuma Haraguchi Anne M. Moon Gen Yamada

Sirenomelia, also known as mermaid syndrome, is a developmental malformation of the caudal body characterized by leg fusion and associated anomalies of pelvic/urogenital organs including bladder, kidney, rectum and external genitalia. Most affected infants are stillborn, and the few born alive rarely survive beyond the neonatal period. Despite the many clinical studies of sirenomelia in humans,...

Journal: :Development 2005
Lise Zakin Bruno Reversade Hiroki Kuroda Karen M Lyons Eddy M De Robertis

Sirenomelia or mermaid-like phenotype is one of the principal human congenital malformations that can be traced back to the stage of gastrulation. Sirenomelia is characterized by the fusion of the two hindlimbs into a single one. In the mouse, sirens have been observed in crosses between specific strains and as the consequence of mutations that increase retinoic acid levels. We report that the ...

Journal: :Indian Journal of Case Reports 2023

Sirenomelia also called mermaid syndrome is a congenital, rare, lethal, multisystemic human malformation of unknown etiology. The characteristic feature sirenomelia the fusion lower limbs, resulting in appearance mermaid’s tail, and thus name “mermaid syndrome.” This condition characterized by various severe urogenital abnormalities presence singular umbilical cord blood vessel, it more common ...

Journal: :National Journal of Clinical Anatomy 2018

2010
Kanchan Kayastha

The newborn at arrival in emergency room of our institution was hypothermic and cyanosed. Neonate was resuscitated. Clinical examination following resuscitation revealed fused lower segment of the body below pelvis into a single limb with no feet. Posture of the lower torso was that of alphabetic letter L when viewed from the back. There were no openings for urogenital system and anal opening w...

ژورنال: Anatomical Sciences Journal 2006
Amoueian, Sakineh, Farhadi, Farshid, Farzad Nia, Mahdi, Kalantari, Mahmoud, Memar, Bahram, Tayebi Meybodi, Naser,

Sirenomelia is a rare congenital anomaly that characterized by complete or incomplete fusion of lower lims and often associated with various malformations.In this report we describe one case of sirenomelia with multiple malformations including fibular agenesis, complete agenesis of anurectum, external genitalia and urinary tract, Inadditin, there was multiple anomaly upper limbs including ageno...

2012
Bilal Mirza

A case of sirenomelia is being reported who was born in a twin pregnancy and showed different anatomy of lower torso.

2015
Parimala Sirikonda Nalluri Himabindu

Address for Correspondence: Dr. Parimala Sirikonda, Assistant Professor, Department of Anatomy, Bhaskar Medical College, Yenkapally, Moinabad, Telangana, India. E-Mail: [email protected] Sirenomelia also known as mermaid syndrome, characterized by fused lower limbs, is a lethal and rare congenital abnormality. This is an extreme example of caudal regression syndrome caused by vascular steal o...

2013
Zahid Gul Anwar Zeb Jan Fahad Liaqat Huma Ambreen Khan

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 ...

Journal: :Brazilian Medical Students 2022

Introdução: Sirenomelia é uma anomalia congênita rara que afeta a formação dos membros inferiores, normalmente pareados por um único membro ao nível da linha média, geralmente está associada defeitos no trato gênito-urinário. Relato do Caso: Caso de necropsia recém-nascido com diagnóstico ultrassonográfico sirenomelia foi óbito minutos após o nascimento. Entre os achados pós mortem destacam-se:...

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