Annals of Neurology · 2016 · 94 citations · 20 references
Life SciencesNeurologyNeuroscienceHepatologyMitochondrial BiologyTransplant SurgeryLiver DiseaseLiver TransplantationMitochondrial DiseaseMitochondrial DisordersMitochondrial DysfunctionMitochondrial Neurological DisordersLiver Transplantation ManagementMitochondrial EncephalomyopathyMitochondrial HepatopathyMitochondrial Neurogastrointestinal EncephalomyopathyPhosphorylase ActivationPurine Nucleoside Phosphorylase DeficiencyThymidine Nucleotide MetabolismThymidine Phosphorylase Deficiency
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is a fatal, recessive disease caused by mutations in the gene encoding thymidine phosphorylase, leading to reduced enzymatic activity, toxic nucleoside accumulation, and secondary mitochondrial DNA damage. Thymidine phosphorylase replacement has been achieved by allogeneic hematopoietic stem cell transplantation, a procedure hampered by high mortality. Based on high thymidine phosphorylase expression in the liver, a 25-year-old severely affected patient underwent liver transplantation. Serum levels of toxic nucleosides rapidly normalized. At 400 days of follow-up, the patient's clinical conditions are stable. We propose liver transplantation as a new therapy for MNGIE. Ann Neurol 2016;80:448-455.
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OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
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Life Sciences, Genetics, Neurology +17
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)
Michio Hirano, Gabriella Silvestri, D. M. Blake et al. · Neurology · 1994 · 407 citations
Altered Thymidine Metabolism Due to Defects of Thymidine Phosphorylase
Antonella Spinazzola, Ramón Martí, Ichizo Nishino et al. · Journal of Biological Chemistry · 2002 · 236 citations · Full text