Journal article
Diagnosis and management of MNGIE syndrome in children: case report and review of the literature
Journal of pediatric gastroenterology and nutrition, v 35(3), pp 377-383
Sep 2002
PMID: 12352533
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) syndrome is a rare disorder that presents in childhood; however, marked delay in diagnosis is common. We report a case and review the literature describing the typical features that should alert pediatricians to the diagnosis. We also describe a novel management strategy for providing symptomatic relief.
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Details
- Title
- Diagnosis and management of MNGIE syndrome in children: case report and review of the literature
- Creators
- J E Teitelbaum - Department of Pediatrics, Divison of Gastroenteroloy and Nustrition, Monmouth Mediacal Center, MCP Hahnemann Medical School, Long Branch, New Jersey 07740, USA. jteitelbaum@sbhcs.comC B BerdeS NurkoC BuonomoA R Perez-AtaydeV L Fox
- Publication Details
- Journal of pediatric gastroenterology and nutrition, v 35(3), pp 377-383
- Publisher
- Lippincott
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Pediatrics
- Web of Science ID
- WOS:000178098200028
- Scopus ID
- 2-s2.0-0036736426
- Other Identifier
- 991019168983204721
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- Collaboration types
- Domestic collaboration
- Web of Science research areas
- Gastroenterology & Hepatology
- Nutrition & Dietetics
- Pediatrics