Alpers Syndrome
What's New
Last Posted: Jun 08, 2023
- Astrocytic pathology in Alpers' syndrome.
Laura A Smith, et al. Acta neuropathologica communications 2023 0 (1) 86 - The Y831C Mutation of the POLG Gene in Dementia.
Eugenia Borgione, et al. Biomedicines 2023 0 (4) - The presence of anaemia negatively influences survival in patients with POLG disease.
Hikmat Omar, et al. Journal of inherited metabolic disease 2017 0 (6) 861-866 - Variations of mitochondrial DNA polymerase ? in patients with Parkinson's disease.
Ylönen S, et al. Journal of neurology 2013 12 (12) 3144-9 - Alpers syndrome
From NCATS Genetic and Rare Diseases Information Center
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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