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Genetics of enteric neuropathies.
Brosens, Erwin; Burns, Alan J; Brooks, Alice S; Matera, Ivana; Borrego, Salud; Ceccherini, Isabella; Tam, Paul K; García-Barceló, Maria-Mercè; Thapar, Nikhil; Benninga, Marc A; Hofstra, Robert M W; Alves, Maria M.
Afiliación
  • Brosens E; Department of Clinical Genetics, Erasmus University Medical Centre - Sophia Children's Hospital, Rotterdam, The Netherlands. Electronic address: e.brosens@erasmusmc.nl.
  • Burns AJ; Department of Clinical Genetics, Erasmus University Medical Centre - Sophia Children's Hospital, Rotterdam, The Netherlands; Stem Cells and Regenerative Medicine, Birth Defects Research Centre, UCL Institute of Child Health, London, UK.
  • Brooks AS; Department of Clinical Genetics, Erasmus University Medical Centre - Sophia Children's Hospital, Rotterdam, The Netherlands.
  • Matera I; UOC Medical Genetics, Istituto Giannina Gaslini, Genova, Italy.
  • Borrego S; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), Seville, Spain; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.
  • Ceccherini I; UOC Medical Genetics, Istituto Giannina Gaslini, Genova, Italy.
  • Tam PK; Division of Paediatric Surgery, Department of Surgery, Li Ka Shing Faculty of Medicine of the University of Hong Kong, Hong Kong, China.
  • García-Barceló MM; State Key Laboratory of Brain and Cognitive Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China; Centre for Reproduction, Development, and Growth, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Thapar N; Stem Cells and Regenerative Medicine, Birth Defects Research Centre, UCL Institute of Child Health, London, UK.
  • Benninga MA; Pediatric Gastroenterology, Emma Children's Hospital/Academic Medical Center, Amsterdam, The Netherlands.
  • Hofstra RM; Department of Clinical Genetics, Erasmus University Medical Centre - Sophia Children's Hospital, Rotterdam, The Netherlands; Stem Cells and Regenerative Medicine, Birth Defects Research Centre, UCL Institute of Child Health, London, UK.
  • Alves MM; Department of Clinical Genetics, Erasmus University Medical Centre - Sophia Children's Hospital, Rotterdam, The Netherlands.
Dev Biol ; 417(2): 198-208, 2016 09 15.
Article en En | MEDLINE | ID: mdl-27426273
Abnormal development or disturbed functioning of the enteric nervous system (ENS), the intrinsic innervation of the gastrointestinal tract, is associated with the development of neuropathic gastrointestinal motility disorders. Here, we review the underlying molecular basis of these disorders and hypothesize that many of them have a common defective biological mechanism. Genetic burden and environmental components affecting this common mechanism are ultimately responsible for disease severity and symptom heterogeneity. We believe that they act together as the fulcrum in a seesaw balanced with harmful and protective factors, and are responsible for a continuum of symptoms ranging from neuronal hyperplasia to absence of neurons.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sistema Nervioso Entérico / Tracto Gastrointestinal / Interacción Gen-Ambiente / Motilidad Gastrointestinal Límite: Humans Idioma: En Revista: Dev Biol Año: 2016 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sistema Nervioso Entérico / Tracto Gastrointestinal / Interacción Gen-Ambiente / Motilidad Gastrointestinal Límite: Humans Idioma: En Revista: Dev Biol Año: 2016 Tipo del documento: Article