Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

last update : 18-05-2010

Symbol	OLEN
Location	15q26.1
Name	occipital lobe epilepsy with nystagmus
Corresponding gene	POLG
Main clinical features	epileptic syndrome with initial features of occipital lobe epilepsy occipital seizure phenomena included flickering coloured light, sometimes persisting for weeks, months or even years, ictal visual loss, horizontal/vertical nystagmus or oculoclonus, dysmorphopsia, micro-/macropsia and palinopsia
Genetic determination	autosomal recessive
Function/system disorder	neurology
Type	disease

Remark(s)