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Intensive nutrition support may benefit patients with a rare mitochondrial disorder.

Arezina KastiMaroulla D NikolakiIoannis PyrousisKalliopi SynodinouNikolaos OikonomopoulosKonstantinos Triantafyllou
Published in: Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition (2021)
Mitochondrial neurogastrointestinal encephalopathy (MNGIE) is a rare, inherited, multisystemic autosomal recessive disorder caused by mutations in the nuclear TYMP gene. This syndrome is characterized by ptosis, external ophthalmoplegia, gastrointestinal dysmotility, cachexia, peripheral neuropathy, and leukoencephalopathy. Our case illustrates a patient diagnosed with MNGIE and cachexia who has benefited from the initiation and maintenance of parenteral nutrition. We highlight the benefits of receiving long-term supplementary home parenteral nutrition under close monitoring for patients with this neurogastrointestinal disease in order to gain weight and maintain good health.
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