8A60.A
category
Epilepsy due to genetic syndromes with widespread or progressive effects
Definition
Epilepsy due to genetically determined conditions in which, as we currently understand it, there is a separate disorder interposed between the genetic defect and the epilepsy, for example, as in tuberous sclerosis. Includes epilepsy due to documented autosomal, X-linked, mitochondrial or chromosomal abnormalities.
Also indexed as
Epilepsy due to X-linked recessive progressive myoclonic epilepsy with ataxiaEpilepsy due to autosomal dominant genetic syndromes with widespread or progressive effectsEpilepsy due to autosomal recessive genetic syndromes with widespread or progressive effectsEpilepsy due to chromosomal disordersEpilepsy due to genetic syndromes with widespread or progressive effectsEpilepsy due to mitochondrial disordersMitochondrial encephalomyopathies
Nearby in Epilepsy due to structural or metabolic conditions or diseases
8A60.0Epilepsy due to prenatal or perinatal brain insults8A60.1Epilepsy due to cerebrovascular disorders8A60.2Epilepsy due to degenerative brain disorders8A60.3Epilepsy due to dementias8A60.4Epilepsy due to central nervous system infections or infestations8A60.5Epilepsy due to injuries to the head8A60.6Epilepsy due to tumours of the nervous system8A60.7Epilepsy with mesial temporal sclerosis