A locus for simple pure febrile seizures maps to chromosome 6q22-q24
نویسندگان
چکیده
منابع مشابه
Novel locus on chromosome 12q22-q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures.
I diopathic epilepsies have a genetic basis and are characterised by the absence of an overt underlying neurological abnormality. Most idiopathic epilepsies are complex diseases with considerable clinical and genetic heterogeneity and an unclear inheritance pattern because of genetic and environmental factors. Families in which the disease segregates as an autosomal dominant trait with reduced ...
متن کاملA locus for primary ciliary dyskinesia maps to chromosome 19q.
Primary ciliary dyskinesia is an autosomal recessive condition characterised by chronic sinusitis, bronchiectasis, and subfertility. Situs inversus occurs in 50% of cases (Kartagener syndrome). It has an estimated incidence of 1 in 20 000 live births. The clinical phenotype is caused by defective ciliary function associated with a range of ultrastructural abnormalities including absent dynein a...
متن کاملCorrelation of Serum Zinc Level with Simple Febrile Seizures: A Hospital based Prospective Case Control Study
Background: Febrile seizures are one of the most common neurological conditions of childhood. It seems that zinc deficiency is associated with increased risk of febrile seizures.Aim: To estimate the serum Zinc level in children with simple Febrile seizures and to find the correlation between serum zinc level and simple Febrile seizures.Materials and Methods: The proposed study was a hospital ba...
متن کاملIron Deficiency as a Risk Factor for Simple Febrile Seizures
Objectives: To determine the association between iron status and febrile seizure. Patients and Methods: This case-control study was conducted among 120 children of age group 6 months to 3 years and hospitalized for the first episode of Febrile Seizures (FS). The case group was compared to a group of 80 ageand sexmatched controls admitted with the same diagnosis of infection but without seizure....
متن کاملIdentification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorder.
BACKGROUND Aortic aneurysms cause significant mortality, and >20% relate to hereditary disorders. Familial aortic aneurysm (FAA) has been described in such conditions as the Marfan and Ehlers-Danlos type IV syndromes, due to defects in the fibrillin-1 and type III procollagen genes, respectively. Other gene defects that cause isolated aneurysms, however, have not thus far been described. METH...
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ژورنال
عنوان ژورنال: Brain
سال: 2002
ISSN: 1460-2156
DOI: 10.1093/brain/awf281