The use of magnetic resonance imaging in the study of asymptomatic familial multiple sclerosis patients

被引:3
|
作者
Barakat-Shrem, O
Fernández-Pérez, MJ
Benavente-Fernández, A
García-Moreno, JM
Ruiz-Peña, JL
Fajardo-Gálvez, J
Izquierdo, G
机构
[1] Hosp Infanta Elena, Serv Med Interns, E-21080 Huelva, Spain
[2] Hosp Infanta Elena, Med Interna Serv, E-21080 Huelva, Spain
[3] Hosp Virgen Macarena, Serv Neurol, Seville, Spain
[4] Hosp Virgen Macarena, Serv Med Intensiva, Seville, Spain
关键词
familial multiple sclerosis; healthy carrier; magnetic resonance imaging;
D O I
10.33588/rn.3709.2003013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction. The multiple sclerosis (MS) is the neurological non traumatical disease, that produces permanent incapacity in the young people with more frequency. A consensus, almost total exists, on the implication of environmental and genetic factors in the pathogenesis of the disease. In a considerable percentage of patients, antecedent relatives of other cases of MS exist, who are separated by other healthy relatives sometimes. Aims. We try to study the familiar antecedents of the MS patients, to locate to the healthy members of the family including in the forced line of the possible genetic transmission of the disease and discarding subclinical affectation by the use of magnetic resonance imaging (RMI). Patients and methods. We reviewed the familiar antecedents of the patients with MS followed by the Unit of MS of the Service of Neurology of the Hospital Virgen Macarena of Seville. After the accomplishment of its genealogical trees, we identified the cases of familial MS. We locate and practice RMI to the healthy subjects of the family, who are in the genetic line of communication of the disease (forced carriers). Results and conclusions. We were able to identify 14 forced carriers of the gene in 12 of the families. In the RMI that were done, we found MS compatible injuries in 10 subjects. These findings confirm the existence of silent forms of the disease, that make difficult the knowledge of the genetic implication in the pathogenesis of the disease.
引用
收藏
页码:811 / 814
页数:4
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