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- Benign_familial_infantile_epilepsy abstract "Benign familial infantile epilepsy (BFIE), also known as benign familial infantile seizures (BFIS) or benign familial infantile convulsions (BFIC) is an epilepsy syndrome. Affected children, who have no other health or developmental problems, develop seizures during infancy. These seizures have focal origin within the brain but may then spread to become generalised seizures. The seizures may occur several times a day, often grouped in clusters over one to three days followed by a gap of one to three months. Treatment with anticonvulsant drugs is not necessary but they are often prescribed and are effective at controlling the seizures. This form of epilepsy resolves after one or two years, and appears to be completely benign. The EEG of these children, between seizures, is normal. The brain appears normal on MRI scan.A family history of epilepsy in infancy distinguishes this syndrome from the non-familial classification (see benign infantile epilepsy), though the latter may be simply sporadic cases of the same genetic mutations. The condition is inherited with an autosomal dominant transmission. There are several genes responsible for this syndrome, on chromosomes 2, 16 and 19. It is generally described as idiopathic, meaning that no other neurological condition is associated with it or causes it. However, there are some forms that are linked to neurological conditions. One variant known as infantile convulsions and choreoathetosis (ICCA) forms an association between BFIE and paroxysmal kinesigenic choreoathetosis and has been linked to the PRRT2 gene on chromosome 16. An association with some forms of familial hemiplegic migraine (FHM) has also been found. Benign familial infantile epilepsy is not genetically related to benign familial neonatal epilepsy (BFNE), which occurs in neonates. However, a variation with seizure onset between two days and seven months called benign familial neonatal–infantile seizures (BFNIS) has been described, which is due to a mutation in the SCN2A gene.".
- Benign_familial_infantile_epilepsy meshId "C535467".
- Benign_familial_infantile_epilepsy wikiPageID "34965466".
- Benign_familial_infantile_epilepsy wikiPageLength "3539".
- Benign_familial_infantile_epilepsy wikiPageOutDegree "15".
- Benign_familial_infantile_epilepsy wikiPageRevisionID "481497735".
- Benign_familial_infantile_epilepsy wikiPageWikiLink Anticonvulsant.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Autosomal_dominant.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Benign_familial_neonatal_epilepsy.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Benign_familial_neonatal_seizures.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Benign_infantile_epilepsy.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Category:Epilepsy_types.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Dominance_(genetics).
- Benign_familial_infantile_epilepsy wikiPageWikiLink EEG.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Electroencephalography.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Epilepsy.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Familial_hemiplegic_migraine.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Focal_seizures.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Infancy.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Infant.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Infantile_convulsions_and_choreoathetosis.
- Benign_familial_infantile_epilepsy wikiPageWikiLink MRI.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Magnetic_resonance_imaging.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Nav1.2.
- Benign_familial_infantile_epilepsy wikiPageWikiLink PRRT2.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Paroxysmal_kinesigenic_choreoathetosis.
- Benign_familial_infantile_epilepsy wikiPageWikiLink Partial_seizure.
- Benign_familial_infantile_epilepsy wikiPageWikiLink SCN2A.
- Benign_familial_infantile_epilepsy wikiPageWikiLinkText "Benign familial infantile epilepsy".
- Benign_familial_infantile_epilepsy wikiPageWikiLinkText "benign familial infantile epilepsy".
- Benign_familial_infantile_epilepsy wikiPageWikiLinkText "infantile convulsions".
- Benign_familial_infantile_epilepsy hasPhotoCollection Benign_familial_infantile_epilepsy.
- Benign_familial_infantile_epilepsy meshid "535467.0".
- Benign_familial_infantile_epilepsy name "Benign familial infantile epilepsy".
- Benign_familial_infantile_epilepsy wikiPageUsesTemplate Template:Infobox_disease.
- Benign_familial_infantile_epilepsy wikiPageUsesTemplate Template:Reflist.
- Benign_familial_infantile_epilepsy subject Category:Epilepsy_types.
- Benign_familial_infantile_epilepsy hypernym Syndrome.
- Benign_familial_infantile_epilepsy type Disease.
- Benign_familial_infantile_epilepsy type Type.
- Benign_familial_infantile_epilepsy type Type.
- Benign_familial_infantile_epilepsy type Thing.
- Benign_familial_infantile_epilepsy type Q12136.
- Benign_familial_infantile_epilepsy comment "Benign familial infantile epilepsy (BFIE), also known as benign familial infantile seizures (BFIS) or benign familial infantile convulsions (BFIC) is an epilepsy syndrome. Affected children, who have no other health or developmental problems, develop seizures during infancy. These seizures have focal origin within the brain but may then spread to become generalised seizures.".
- Benign_familial_infantile_epilepsy label "Benign familial infantile epilepsy".
- Benign_familial_infantile_epilepsy sameAs m.0j437m3.
- Benign_familial_infantile_epilepsy sameAs Q4887955.
- Benign_familial_infantile_epilepsy sameAs Q4887955.
- Benign_familial_infantile_epilepsy wasDerivedFrom Benign_familial_infantile_epilepsy?oldid=481497735.
- Benign_familial_infantile_epilepsy isPrimaryTopicOf Benign_familial_infantile_epilepsy.
- Benign_familial_infantile_epilepsy name "Benign familial infantile epilepsy".