Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier.

Nass, Robert Daniel

Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier. [electronic resource] - Seizure Mar 2019 - 1-3 p. digital

Publication Type: Case Reports; Letter

1532-2688

10.1016/j.seizure.2019.01.029 doi


Adult
Epilepsies, Partial--diagnosis
GTP Phosphohydrolases--genetics
Heterozygote
Humans
Male
Mitochondrial Diseases--diagnosis
Retinal Diseases--diagnosis