MovDisordV3, Main, Exploration, bibRecord, 006161

Intrafamilial correlation in idiopathic torsion dystonia

Identifieur interne : 006161 ( Main/Exploration ); précédent : 006160; suivant : 006162

Intrafamilial correlation in idiopathic torsion dystonia

Auteurs : Fletcher [Royaume-Uni] ; A. E. Harding [Royaume-Uni] ; C. D. Marsden [Royaume-Uni]

Source :

Movement Disorders [ 0885-3185 ] ; 1991.

RBID : ISTEX:C9AC21C9DC4E80145C20BFF3B9D5939B31B77793

Descripteurs français

Wicri :
- topic : Génétique.

English descriptors

KwdEn :
- Adolescent, Adult, Analysis of Variance, Child, Dystonia, Dystonia Musculorum Deformans (diagnosis), Dystonia Musculorum Deformans (genetics), Female, Genetics, Heterogeneity, Heterozygote Detection, Humans, Jews (genetics), Male, Middle Aged, Models, Genetic, Risk Factors.
MESH :
- diagnosis : Dystonia Musculorum Deformans.
- genetics : Dystonia Musculorum Deformans, Jews.
- Adolescent, Adult, Analysis of Variance, Child, Female, Heterozygote Detection, Humans, Male, Middle Aged, Models, Genetic, Risk Factors.

Abstract

Age of onset and severity of idiopathic torsion dystonia (ITD) were studied in 100 British families containing 107 index cases and 79 secondary cases. Analysis of variance of these clinical features did not suggest that ITD is genetically heterogenous, and they were similar in Jewish and non‐Jewish patients. Intrafamilial correlation for age of onset was low, particularly between parents and their offspring, suggesting that the ITD phenotype may be determined in part by nongenetic factors or an allelic modifying gene.

Url:

https://api.istex.fr/document/C9AC21C9DC4E80145C20BFF3B9D5939B31B77793/fulltext/pdf

DOI: 10.1002/mds.870060407

Affiliations:

Le document en format XML

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<term>Dystonia Musculorum Deformans (diagnosis)</term>
<term>Dystonia Musculorum Deformans (genetics)</term>
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<term>Genetics</term>
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<term>Heterozygote Detection</term>
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<front><div type="abstract" xml:lang="en">Age of onset and severity of idiopathic torsion dystonia (ITD) were studied in 100 British families containing 107 index cases and 79 secondary cases. Analysis of variance of these clinical features did not suggest that ITD is genetically heterogenous, and they were similar in Jewish and non‐Jewish patients. Intrafamilial correlation for age of onset was low, particularly between parents and their offspring, suggesting that the ITD phenotype may be determined in part by nongenetic factors or an allelic modifying gene.</div>
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Movement Disorders (revue)

Intrafamilial correlation in idiopathic torsion dystonia

Intrafamilial correlation in idiopathic torsion dystonia

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.