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Article

Benign infantile familial convulsions: natural history of a case and clinical characteristics of a large Italian family.

Neuropediatrics - 1 Apr 1999

Giordano L, Accorsi P, Valseriati D, Tiberti A, Menegati E, Zara F, Vignoli A, Vigevano F

Abstract excerpt

We present a patient (3 months old) with partial and generalized seizures who has a family history of seizures with a onset during the first 12 months of life. We diagnosed benign infantile familial convulsions (BIFC) and we did not introduce any antiepileptic therapy. We present clinical data of her family where 18 out of 35 members were affected; to our knowledge this is the largest family with BIFC. BIFC is...

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Source

Identifiers

PMID: 10401694
DOI: 10.1055/s-2007-973469

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Benign infantile familial convulsions: natural history of a case and clinical characteristics of a large Italian family.PMID 10401694Read ↗

Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q.Semantic proximity Read ↗

No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1.Semantic proximity Read ↗

Benign infantile familial convulsions are not an allelic form of the benign familial neonatal convulsions gene.Semantic proximity Read ↗

Benign familial infantile convulsions: linkage to chromosome 16p12-q12 in 14 families.Semantic proximity Read ↗

Positive association between benign familial infantile convulsions and LGI4.Semantic proximity Read ↗

Benign familial infantile convulsions: phenotypic variability in a family.Semantic proximity Read ↗

[Familial and non-familial benign infantile seizures: A homogeneous entity?].Semantic proximity Read ↗

A novel SCN2A mutation in family with benign familial infantile seizures.Semantic proximity Read ↗

Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families.Semantic proximity Read ↗

Refinement of the chromosome 16 locus for benign familial infantile convulsions.Semantic proximity Read ↗

Etiologies, outcomes, and risk factors for epilepsy in infants: a case-control study.Semantic proximity Read ↗

Study of the voltage-gated sodium channel beta 1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC).Semantic proximity Read ↗

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