Ferrera Loretta, Caponnetto Claudia, Marini Valeria, Rizzi Domenica, Bordo Domenico, Penco Silvana, Amoroso Antonio, Origone Paola, Garrè Cecilia
Department of Oncology, Biology and Genetics University of Genova, Genova, Italy.
Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):167-70. doi: 10.1080/aml.4.3.167.170.
Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurological disease. Mutations of the Cu/Zn superoxide dismutase gene (SOD1) are responsible for 20% of autosomal dominant familial ALS (FALS).
We examined the clinical features of the first Italian FALS with the Leu144Phe SOD1 mutation. Seven affected members were identified in a six-generation pedigree. A slowly progressive course (20.4+/-14.6 years) was observed in five patients. One patient died of cardiac failure two years after the onset of the disease. The propositus is still alive. Neurological manifestations began in the legs in all patients, while bulbar signs were absent or appeared late in the course of the disease.
There is evidence of a correlation between this mutation and a slowly progressive phenotype of ALS. Moreover this rare mutation might derive from a common ancestor.
肌萎缩侧索硬化症(ALS)是一种进行性致命性神经疾病。铜/锌超氧化物歧化酶基因(SOD1)突变导致20%的常染色体显性遗传性ALS(FALS)。
我们研究了首例携带Leu144Phe SOD1突变的意大利FALS患者的临床特征。在一个六代家系中鉴定出7名患病成员。5名患者病程进展缓慢(20.4±14.6年)。1例患者在发病两年后死于心力衰竭。先证者仍然存活。所有患者的神经症状均始于腿部,而延髓症状在病程中未出现或出现较晚。
有证据表明该突变与ALS的缓慢进展表型之间存在关联。此外,这种罕见突变可能源自共同祖先。