Literature DB >> 1815594

Genetic studies of febrile convulsions: analysis of twin and family data.

T Tsuboi1, S Endo.   

Abstract

Children with febrile convulsions (FC) including 46 twin pairs, 1913 families including 393 sibling pairs, and 42 three-generation FC kindreds have been studied. Twin studies: (1) The pairwise concordance rate for FC was 69% (18/26 pairs) in monozygotic (MZ) and 20% (4/20 pairs) in dizygotic (DZ) twins (P less than 0.01). (2) The intra-pair similarity of clinical symptoms in 18 concordant MZ twin pairs showed a positive significant correlation, particularly in 4 items--duration of seizure, exogenous factors, intelligence level, and background EEG abnormality. These correlations were greater than those in sibling pairs. (3) No evident cause for discordance was detected in 8 discordant MZ twin pairs, and many dissimilar symptoms were observed in 4 concordant DZ twin pairs. Sibship studies: A large positive correlation of some clinical symptoms was observed in sibling pairs concordant for FC: age at onset of FC, degree of fever, duration of seizure, exogenous factors, and background EEG abnormality (r = +0.2- +0.6). Family history analysis: Morbidity risk among near relatives (17% in parents, 23% in siblings) than in second- (6.1%) or third-degree relatives (4.6%). The difference was found between: sibling greater than parents, uncles greater than aunts, male cousins greater than female cousins. Segregation analysis showed maternal preponderance. In 42 three-generation kindreds the morbidity risk was higher in siblings (32%), uncles/aunts (14%), and cousins (6.4%) than in relatives of other probands. Characteristic findings in FC patients with family history: Characteristic findings in FC patients with an FC parent or sibling, compared with those with no family history, were early onset of FC, lower degree of fever, longer duration of seizure, many recurrences, FC recurrence after age 3, and background EEG abnormality. Similar findings were more markedly observed in 42 3-generation kindreds. Mode of inheritance: A multifactorial mode of inheritance for FC receives some support from this study, and the heritability was estimated as 75%.

Entities:  

Mesh:

Year:  1991        PMID: 1815594

Source DB:  PubMed          Journal:  Epilepsy Res Suppl        ISSN: 0922-9833


  8 in total

1.  Interleukin 1 beta -511 C/T gene polymorphism and susceptibility to febrile seizures: a meta-analysis.

Authors:  Zhen-Qiang Wu; Liang Sun; Ye-Huan Sun; Cizao Ren; Yu-Hong Jiang; Xiao-Ling Lv
Journal:  Mol Biol Rep       Date:  2011-12-13       Impact factor: 2.316

2.  Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation.

Authors:  Liesbet Deprez; Lieve R F Claes; Kristl G Claeys; Dominique Audenaert; Tine Van Dyck; Dirk Goossens; Wim Van Paesschen; Jurgen Del-Favero; Christine Van Broeckhoven; Peter De Jonghe
Journal:  Hum Genet       Date:  2005-11-05       Impact factor: 4.132

3.  Febrile seizures: an appropriate-aged model suitable for long-term studies.

Authors:  T Z Baram; A Gerth; L Schultz
Journal:  Brain Res Dev Brain Res       Date:  1997-02-20

4.  Early-life febrile seizures worsen adult phenotypes in Scn1a mutants.

Authors:  Stacey B B Dutton; Karoni Dutt; Ligia A Papale; Sandra Helmers; Alan L Goldin; Andrew Escayg
Journal:  Exp Neurol       Date:  2017-04-01       Impact factor: 5.330

5.  A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.

Authors:  S Baulac; I Gourfinkel-An; F Picard; M Rosenberg-Bourgin; J F Prud'homme; M Baulac; A Brice; E LeGuern
Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

6.  Epilepsy in families: Age at onset is a familial trait, independent of syndrome.

Authors:  Colin A Ellis; Leonid Churilov; Michael P Epstein; Sharon X Xie; Susannah T Bellows; Ruth Ottman; Samuel F Berkovic
Journal:  Ann Neurol       Date:  2019-05-20       Impact factor: 10.422

7.  Epilepsy After Febrile Seizures: Twins Suggest Genetic Influence.

Authors:  Syndi A Seinfeld; John M Pellock; Marianne J Kjeldsen; Karl Otto Nakken; Linda A Corey
Journal:  Pediatr Neurol       Date:  2015-10-31       Impact factor: 3.372

8.  Lack of association between TNF-α gene polymorphisms at position -308 A, -850T and risk of simple febrile convulsion in pediatric patients.

Authors:  Abolfazl Khoshdel; Soleman Kheiri; Roya Habibian; Ahora Nozari; Azar Baradaran
Journal:  Adv Biomed Res       Date:  2012-12-28
  8 in total

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