brain disorder Metabolic disease with intestinal involvement Genetic neurodegenerative disease Mitochondrial myopathy Mitochondrial disease with peripheral neuropathy Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies Alpers syndrome MESH:D002549 ALPERS-HUTTENLOCHER SYNDROME Alpers-Huttenlocher syndrome Sirarat Sarntivijai Alper's syndrome ICD10:G31.8 progressive sclerosing poliodystrophy (disorder) ALPERS PROGRESSIVE INFANTILE POLIODYSTROPHY A cerebral degeneration that results in progressive degeneration of grey matter in the cerebrum and has_symptom convulsions. DOID:1442 Alpers' disease or gray-matter degeneration MedDRA:10062943 Alpers progressive sclerosing poliodystrophy Diffuse Cerebral Sclerosis of Schilder OMIM:203700 MITOCHONDRIAL DNA DEPLETION SYNDROME 4A UMLS:C0205710 Progressive neuronal degeneration of childhood with liver disease Mitochondrial disease with eye involvement