Digestive tract disorders revealing mitochondrial cytopathy: MNGIE syndrome;Cas clinique troubles digestifs révélateurs d'une cytopathie mitochondriale: Le syndrome MNGIE

Revue Neurologique

Volumn 158, Issue 1, 2002, Pages 111-113

  Chaury, F ^a   Fleury, M ^a   Tranchant, C ^a  

^a UNIVERSITY HOSPITAL OF STRASBOURG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; SUCCINATE DEHYDROGENASE;

ADULT; ARTICLE; CASE REPORT; COLONOSCOPY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTROMYOGRAPHY; GASTROINTESTINAL DISEASE; GASTROSCOPY; HUMAN; MALE; MNGIE SYNDROME; MUSCLE BIOPSY; NUCLEAR MAGNETIC RESONANCE IMAGING; POLYNEUROPATHY; SYNDROME; DIGESTIVE SYSTEM DISEASE; MITOCHONDRIAL ENCEPHALOMYOPATHY;

ADULT; DIGESTIVE SYSTEM DISEASES; HUMANS; MALE; MITOCHONDRIAL ENCEPHALOMYOPATHIES; SYNDROME;

EID: 0036372808     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Le MNGIE syndrome: Deux cas dans une même fratrie Rev
2. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Clinical, biochimical, and genetic features of an autosomal recessive mitochondrial disorder
3. Mitochondrial neurogastrointestinal encephalomyopathy syndrom chromosome 22q13.32-qter
4. Mitochondrial neurogastrointestinal recessive disorder due to thymidine phosphorylase mutations
5. MNGIE: From nuclear DNA to mtDNA