Mitochondrial neurogastrointestinal encephalomyopathy

MONDO:0017575

A syndrome characterized by the association of gastrointestinal dysmotility, peripheral neuropathy, chronic progressive external ophthalmoplegia and leukoencephalopathy.

Also known as: MNGIE, Mitochondrial Neurogastrointestinal Encephalopathy, Mitochondrial neurogastrointestinal encephalopathy, mitochondrial Neurogastrointestingal encephalopathy, MNGIE syndrome, OGIMD, POLIP, mitochondrial neurogastrointestinal encephalopathy syndrome

27 clinical trials for this condition and its sub-types.

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Sub-types

Mitochondrial DNA depletion syndrome 1 (0) Mitochondrial DNA depletion syndrome 20 (mngie type) (0) Mitochondrial DNA depletion syndrome 4b (0) Mitochondrial DNA depletion syndrome 8a (0)

Broader categories

Disease (680) Metabolic disease (233) Nervous system disorder (231) Musculoskeletal system disorder (207) Hereditary disease (176) Peripheral nervous system disorder (114) Neuromuscular disease (106) Peripheral neuropathy (91) Inborn mitochondrial metabolism disorder (58) Muscle tissue disorder (56)

Trials to join now! 16 Not yet recruiting 1 Not yet finished but already full! 5 Completed 3 Terminated 2

Mitochondrial neurogastrointestinal encephalomyopathy

Sub-types

Broader categories

New drug aims to tame hard-to-control seizures in rare mitochondrial disorders

Could a simple blood test track nerve damage? a study investigates NT-3 levels in neuropathy.