Benign infantile familial convulsions are not an allelic form of the benign familial neonatal convulsions gene.

Abstract

Benign infantile familial convulsions (BIFC) and benign familial neonatal convulsions (BFNC) are two forms of familial convulsions having an age of onset within the first year of life. The gene responsible for BFNC has been mapped to chromosome 20q in the close vicinity of D20S19 and D20S20 markers. We performed linkage analysis between BIFC and D20S19-D20S20 in eight families in order to know whether the BFNC gene is also implicated in BIFC. Several apparent obligate crossovers between affected members were detected. The data here presented demonstrate that the BFNC gene is not responsible for BIFC.

• Authors: A Malafosse, C Beck, H Bellet, M Di Capua, O Dulac, B Echenne, L Fusco, P Lucchini, S Ricci, R Sebastianelli
• Journal: Annals of neurology (Ann Neurol) Vol. 35 Issue 4 Pg. 479-82 (Apr 1994) ISSN: 0364-5134 [Print] United States
• PMID: 8154876 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• DNA

Topics

• Age of Onset
• Alleles
• Child, Preschool
• DNA (analysis)
• Female
• Genetic Linkage
• Humans
• Lod Score
• Male
• Pedigree
• Seizures (genetics)