نتایج جستجو برای: anorectal malformation

تعداد نتایج: 17722  

Journal: :Translational Gastroenterology and Hepatology 2021

Journal: :Journal of Neonatal Surgery 2012

Journal: :Journal of Indian Association of Pediatric Surgeons 2017

Journal: :Genes & development 2008
Dorota Szumska Guido Pieles Rachid Essalmani Michal Bilski Daniel Mesnard Kulvinder Kaur Angela Franklyn Kamel El Omari Joanna Jefferis Jamie Bentham Jennifer M Taylor Jurgen E Schneider Sebastian J Arnold Paul Johnson Zuzanna Tymowska-Lalanne Dave Stammers Kieran Clarke Stefan Neubauer Andrew Morris Steve D Brown Charles Shaw-Smith Armando Cama Valeria Capra Jiannis Ragoussis Daniel Constam Nabil G Seidah Annik Prat Shoumo Bhattacharya

We have identified an ethylnitrosourea (ENU)-induced recessive mouse mutation (Vcc) with a pleiotropic phenotype that includes cardiac, tracheoesophageal, anorectal, anteroposterior patterning defects, exomphalos, hindlimb hypoplasia, a presacral mass, renal and palatal agenesis, and pulmonary hypoplasia. It results from a C470R mutation in the proprotein convertase PCSK5 (PC5/6). Compound muta...

2018
V Upadhyaya A Gangopadhyay P Srivastava Z Hasan S Sharma

Introduction: Anorectal malformations comprise a wide spectrum of diseases, which can affect boys and girls, and involve the distal anus and rectum as well as the urinary and genital tracts. They occur in approximately 1 in 3500 to 5000 live births. Since the early era of its management, its treatment has gone through an enormous phase of evolution leading from gloomy outcome in the past to nea...

Journal: :Journal of medical genetics 2000
S A Lynch Y Wang T Strachan J Burn S Lindsay

Autosomal dominant sacral agenesis is characterised by a partial agenesis of the sacrum typically involving sacral vertebrae S2-S5 only. Associated features include anorectal malformation, a presacral mass, and urogenital malformation. Together, these features have been defined as the Currarino syndrome. Recently, HLXB9 has been identified as the major causative gene in Currarino syndrome allow...

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