نتایج جستجو برای: anorectal malformation

تعداد نتایج: 17722  

Journal: :Journal of Pediatric Surgery Case Reports 2020

Journal: :Journal of Indian Association of Pediatric Surgeons 2011

Journal: : 2023

The article deals with anorectal malformation, which is a congenital anomaly in animals. This malformation often combined other birth defects and requires comprehensive diagnosis patients. Congenital malformations of the gastrointestinal tract are quite rare. Carrying out complex diagnostics before each stage surgical treatment will allow to determine certain method technique correction save pa...

Journal: :Journal of Nepal Paediatric Society 2015

Journal: :Journal of Evolution of Medical and Dental Sciences 2016

2013
Shin Yun Byun Ryoung Kyoung Lim Kyung Hee Park Yong Hoon Cho Hae Young Kim

PURPOSE Anorectal malformations are often associated with other anomalies, reporting frequency with 40-70%. Gastrointestinal anomalies have been known to be relatively less common than associated anomalies of other organ system. This study was performed to assess a distinctive feature of cases associated with esophageal atresia. METHODS Clinical data (from January 2000 through December 2011) ...

2017
Corine Baayen Fanny Feuillet Pauline Clermidi Célia Crétolle Sabine Sarnacki Guillaume Podevin Jean-Benoit Hardouin

BACKGROUND The Hirschsprung's disease Anorectal malformation QoL questionnaire (HAQL) is a disease-specific quality of life (QoL) questionnaire for patients with Hirschsprung's disease (HD) or anorectal malformations (ARM). It was originally proposed in Dutch and is currently being translated into other languages to obtain an internationally standardized instrument. In this work we validate a F...

2000
Sally Ann Lynch Yiming Wang T Strachan John Burn Susan 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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