Photosensitive epilepsy




Input patient's signs and symptoms


Narrow down the case reports



Total: 23 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
2
(4.0%)
1908752
Language-apparent reflex epilepsy.
Jacome DE.
Clin Electroencephalogr. 1991;22(3):172-7.
Seizure
Absence Epilepsy Electroencephalography Females Homo sapiens Languages Light
2
(4.0%)
1733763
Pattern-sensitive epilepsy: genetic aspects in two families.
Brinciotti M, Trasatti G, Pelliccia A, Matricardi M.
Epilepsia. 1992;33(1):88-92.
Seizure
Brain Child Electroencephalography Epilepsy Family Females Form Perception Homo sapiens Photic Stimulation
2
(4.0%)
403104
Treatment of generalized epilepsies of childhood and adolescence with sodium valproate ("epilim").
Jeavons PM, Clark JE, Maheshwari MC.
Dev Med Child Neurol. 1977;19(1):9-25.
Seizure
Absence Epilepsy Automatism Child Drug Evaluation Electroencephalography Epilepsy Females Homo sapiens Light Male Myoclonic Epilepsy Valerates
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 9

HPO ID Term # of case reports
HP:0001250 Seizures 5
HP:0002121 Absence seizure 2
HP:0000518 Cataract 1
HP:0000726 Dementia 1
HP:0001332 Dystonia 1
HP:0002076 Migraine 1
HP:0002315 Headache 1
HP:0007199 Progressive spastic paraparesis 1
HP:0030521 Bitemporal hemianopia 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID