Results 31 to 40 of about 61,174 (158)
Jurnal Profesi Medika, 2020 Duodenal atresia is an emergency congenital abnormality and the most common cause of proximal bowel obstruction in neonates, where the duodenum has not developed properly in embryogenesis with a blind end that cannot be seen through gastric contents. The
Fiona Fiona +2 more
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Duodenal atresia with major duodenal papilla within duodenal atretic segment: A case report [PDF]
, 2014 Duodenal atresia is a common cause of neonatal bowel obstruction and presents with numerous anomalies. Ampullary anomalies are rare, but one must consider potential abnormalities to both the biliary ductal system and the ampulla of Vater to avoid ...
Stehr, Wolfgang +2 more
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DUODENAL OBSTRUCTION IN CHILDREN: AN EIGHT YEAR EXPERIENCE IN BASRAH [PDF]
Basrah Journal of Surgery, 2017 DUODENAL OBSTRUCTION IN CHILDREN: AN EIGHT YEAR EXPERIENCE IN BASRAH Abbas Abdulzahra Alhasani MB, ChB, FIBMS, MRCS Glasgow, Pediatric Surgeon, Lecturer, Department of Surgery, College of Medicine, University of Basrah, IRAQ.
Abbas Abdulzahra Alhasani
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Congenital short bowel syndrome: Clinical aspects by systematic review
JPGN Reports, EarlyView.Abstract Objectives Congenital short bowel syndrome (CSBS) is a rare intestinal disorder characterized by inborn shortening of the bowel with mainly mutations in Coxsackie and Adenovirus receptor‐like membrane protein (CLMP) and Filamin A (FLNA) genes.
Barblin Remund +2 more
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Obstrução duodenal congênita. [PDF]
, 1999 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Colombeli, Eliete Magda
core
Combined Duodenal Atresia and Pure Esophageal Atresia
, 2015 Combined duodenal atresia and pure esophageal atresia is a rare combination which has been reported only 13 times previously in the literature. Although this pair of congenital anomalies is amenable to current treatment strategies, it is often associated
Alaish SM
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Prenatal Diagnosis, EarlyView.ABSTRACT Objective Trisomy 21 (T21) is associated with various neurological impairments. However, the mechanisms of fetal brain development in T21 and their impact on neurodevelopmental outcomes remain unclear, limiting prenatal counseling. Therefore, this study aims to assess neuropathological changes in fetuses with T21 and the associated ...
Christina Haberl +9 more
wiley +1 more source
Concurrent validity and agreement of Bayley‐4, AIMS, and HINE assessments in 1‐year‐old children
Developmental Medicine &Child Neurology, EarlyView.In this cross‐sectional study of children around 1‐year‐old, the Bayley‐4 showed concurrent validity and moderate to substantial agreement with the AIMS and the HINE in both clinical and home settings. Abstract Aim To examine concurrent validity between the Bayley Scales of Infant and Toddler Development, Fourth Edition (Bayley‐4) gross motor subtest ...
Weiyang Deng +14 more
wiley +1 more source
Laparoscopic Repair of Duodenal Atresia with Annular Pancreas [PDF]
, 2016 Duodenal atresia is the most common cause of congenital bowel obstruction. Often it is associated with other congenital anomalies, such as annular pancreas.
Correia-Pinto, J, Barroso, C
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American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2331-2337, October 2026.ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli +11 more
wiley +1 more source