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The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.
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Alpers Syndrome
Alpers Syndrome
Prevalence:
1/200000
mitochondrial
Official
·
OMIM:203700
Official
·
ORPHA726
Progressive neuronal degeneration and liver failure due to POLG gene mutations.
Associated Genes
POLG
DNA Polymerase Gamma Catalytic Subunit
Chromosome 15
Autosomal Recessive