An Italian dominant FALS Leu144Phe SOD1 mutation:: genotype-phenotype correlation

被引:17
作者
Ferrera, L
Caponnetto, C
Marini, V
Rizzi, D
Bordo, D
Penco, S
Amoroso, A
Origone, P
Garrè, C
机构
[1] Univ Genoa, Dept Oncol Biol & Genet, I-16132 Genoa, Italy
[2] Univ Genoa, Dept Neurosci Ophthalmol & Genet, Genoa, Italy
[3] Natl Inst Canc Res, Genoa, Italy
[4] Osped Niguarda Ca Granda, Div Genet Anal, Milan, Italy
[5] Childrens Hosp, Med Genet Unit, Trieste, Italy
[6] Univ Trieste, Trieste, Italy
来源
AMYOTROPHIC LATERAL SCLEROSIS | 2003年 / 4卷 / 03期
关键词
FALS-SOD1; gene; Leu144Phe mutation; non severe phenotype; common ancestor;
D O I
10.1080/aml.4.3.167.170
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
INTRODUCTION: 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). RESULTS: 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. DISCUSSION: 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.
引用
收藏
页码:167 / 170
页数:4
相关论文
共 16 条
[1]   AMYOTROPHIC-LATERAL-SCLEROSIS AND STRUCTURAL DEFECTS IN CU,ZN SUPEROXIDE-DISMUTASE [J].
DENG, HX ;
HENTATI, A ;
TAINER, JA ;
IQBAL, Z ;
CAYABYAB, A ;
HUNG, WY ;
GETZOFF, ED ;
HU, P ;
HERZFELDT, B ;
ROOS, RP ;
WARNER, C ;
DENG, G ;
SORIANO, E ;
SMYTH, C ;
PARGE, HE ;
AHMED, A ;
ROSES, AD ;
HALLEWELL, RA ;
PERICAKVANCE, MA ;
SIDDIQUE, T .
SCIENCE, 1993, 261 (5124) :1047-1051
[2]   Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation:: Potential impact of CNTF as a candidate modifier gene [J].
Giess, R ;
Holtmann, B ;
Braga, M ;
Grimm, T ;
Müller-Myhsok, B ;
Toyka, KV ;
Sendtner, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (05) :1277-1286
[3]   Superoxide dismutase in CSF from amyotrophic lateral sclerosis patients with and without CuZn-superoxide dismutase mutations [J].
Jacobsson, J ;
Jonsson, PA ;
Andersen, PM ;
Forsgren, L ;
Marklund, SL .
BRAIN, 2001, 124 :1461-1466
[4]   Prognosis in familial amyotrophic lateral sclerosis: Progression and survival in patients with glu100gly and ala4val mutations in Cu,Zn superoxide dismutase [J].
Juneja, T ;
PericakVance, MA ;
Laing, NG ;
Dave, S ;
Siddique, T .
NEUROLOGY, 1997, 48 (01) :55-57
[5]   ALS with variable phenotypes in a six-generation family caused by leu144phe mutation in the SOD1 gene [J].
Masè, G ;
Ros, S ;
Gemma, A ;
Bonfigli, L ;
Carraro, N ;
Cazzato, G ;
Rolfo, M ;
Zanconati, F ;
Sepcic, J ;
Jurjevic, A ;
Pirulli, D ;
Boniotto, M ;
Zezlina, S ;
Crovella, S ;
Amoroso, A .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2001, 191 (1-2) :11-18
[6]   Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with a His46Arg mutation in Cu/Zn superoxide dismutase [J].
Ohi, T ;
Saita, K ;
Takechi, S ;
Nabesima, K ;
Tashiro, H ;
Shiomi, K ;
Sugimoto, S ;
Akematsu, T ;
Nakayama, T ;
Iwaki, T ;
Matsukura, S .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2002, 197 (1-2) :73-78
[7]   Amyotrophic lateral sclerosis: A proposed mechanism [J].
Okado-Matsumoto, A ;
Fridovich, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (13) :9010-9014
[8]   Amyotrophic lateral sclerosis: copper/zinc superoxide dismutase (SOD1) gene mutations [J].
Orrell, RW .
NEUROMUSCULAR DISORDERS, 2000, 10 (01) :63-68
[9]   ATOMIC STRUCTURES OF WILD-TYPE AND THERMOSTABLE MUTANT RECOMBINANT HUMAN CU,ZN SUPEROXIDE-DISMUTASE [J].
PARGE, HE ;
HALLEWELL, RA ;
TAINER, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) :6109-6113
[10]  
Penco, 2001, NEUROLOGY, V57, P1146