Article

Recurrent Abdominal Pain, Vomiting, Velvet-Like Changes in the Small Intestine in a Patient with Multiple Acyl-CoA dehydrogenation Deficiency

2020-08-13

Abstract excerpt

<h4>Background: </h4> Multiple acyl-CoA dehydrogenation deficiency (MADD) is an inborn error of metabolism in fatty acid oxidation. We described an unusual case of recurrent vomiting and abdominal pain in a child with MADD, presenting with velvet-like changes in the small intestine. <h4>Methods: </h4> Because of prominent gastrointestinal manifestations and small intestine ulcers, the patient was first diagnosed a...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 7270ee58-b0b5-55ce-96c9-4ebbed9d68ae
DOI: 10.21203/rs.3.rs-54093/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Recurrent Abdominal Pain, Vomiting, Velvet-Like Changes in the Small Intestine in a Patient with Multiple Acyl-CoA dehydrogenation DeficiencyDOI 10.21203/rs.3.rs-54093/v1Read

A systematic review of late-onset and very-late-onset multiple acyl-coenzyme A dehydrogenase deficiency: Cohort analysis and patient report from Taiwan.Semantic proximity Read

[Analysis of clinical features and genetic variants in three children with late-onset Multiple acyl-Coenzyme A dehydrogenase deficiency].Semantic proximity Read

Vitelline vascular remnant causing intestinal obstruction in a patient with TARP syndrome.Semantic proximity Read

Gastrointestinal Manifestations in Rubinstein-Taybi Syndrome.Semantic proximity Read

Cyclic vomiting and digestive symptoms in White–Sutton syndrome: a participatory studySemantic proximity Read

A Unique Observation of A Patient With Vulto-Van Silfhout-De Vries SyndromeSemantic proximity Read

Novel Genetic Variants Associated with Child Refractory Esophageal Stricture with Food Allergy by Exome Sequencing.Semantic proximity Read

Characterization of a Novel Pathogenic Mutation Causing Mitochondrial Neurogastrointestinal EncephalopathySemantic proximity Read

Late-onset MADD in Yemen caused by a novel ETFDH mutation misdiagnosed as ADEM.Semantic proximity Read

Children with cyclic vomiting syndrome: phenotypes, disease burden and mitochondrial DNA analysis.Semantic proximity Read

Nutritional and gastrointestinal manifestations in Rett syndrome: long-term follow-up.Semantic proximity Read

[Multiple endocrine neoplasia and very early onset inflammatory bowel disease. An unexpected association].Semantic proximity Read