DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex

被引:138
作者
Annesi, G
Savettieri, G
Pugliese, P
D'Amelio, M
Tarantino, P
Ragonese, P
La Bella, V
Piccoli, T
Civitelli, D
Annesi, F
Fierro, B
Piccoli, F
Arabia, G
Caracciolo, M
Candiano, ICC
Quattrone, A
机构
[1] Univ Magne Graecia, Cattedra & UO Neurol, Inst Neurol, I-88100 Catanzaro, Italy
[2] Univ Palermo, Dept Neurol Ophthalmol Otorinolaringol & Psychiat, Palermo, Italy
[3] CNR, Inst Neurol Sci, Cosenza, Italy
关键词
D O I
10.1002/ana.20666
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
DJ-1 gene mutations have been found to cause early-onset Parkinson's disease. We report a family from southern Italy with three brothers affected by early-onset parkinsonism, dementia, and amyotrophic lateral sclerosis. Molecular analysis of the DJ-1 gene in two living patients showed a novel homozygous mutation in exon 7 (E163K) and a new homozygous mutation (g.168_185dup) in the promoter region of the gene. Both mutations cosegregated with the disease and were detected in a heterozygous state in the patients' mother and their healthy siblings. Our findings expand the spectrum of clinical presentations associated with mutations in DJ-1 gene.
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页码:803 / 807
页数:5
相关论文
共 19 条
  • [1] The role of pathogenic DJ-1 mutations in Parkinson's disease
    Abou-Sleiman, PM
    Healy, DG
    Quinn, N
    Lees, AJ
    Wood, NW
    [J]. ANNALS OF NEUROLOGY, 2003, 54 (03) : 283 - 286
  • [2] AMYOTROPHIC LATERAL SCLEROSIS - 50 CASES OBSERVED ON GUAM
    ARNOLD, A
    EDGREN, DC
    PALLADINO, VS
    [J]. JOURNAL OF NERVOUS AND MENTAL DISEASE, 1953, 117 (02) : 135 - 139
  • [3] Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's disease
    Bonifati, V
    Oostra, BA
    Heutink, P
    [J]. JOURNAL OF MOLECULAR MEDICINE-JMM, 2004, 82 (03): : 163 - 174
  • [4] Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
    Bonifati, V
    Rizzu, P
    van Baren, MJ
    Schaap, O
    Breedveld, GJ
    Krieger, E
    Dekker, MCJ
    Squitieri, F
    Ibanez, P
    Joosse, M
    van Dongen, JW
    Vanacore, N
    van Swieten, JC
    Brice, A
    Meco, G
    van Duijn, CM
    Oostra, BA
    Heutink, P
    [J]. SCIENCE, 2003, 299 (5604) : 256 - 259
  • [5] El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis
    Brooks, BR
    Miller, RG
    Swash, M
    Munsat, TL
    [J]. AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS, 2000, 1 (05): : 293 - 299
  • [6] BUEESCHERRER V, 1995, AM J PATHOL, V146, P924
  • [7] Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
    Clark, LN
    Poorkaj, P
    Wszolek, Z
    Geschwind, DH
    Nasreddine, ZS
    Miller, B
    Li, D
    Payami, H
    Awert, F
    Markopoulou, K
    Andreadis, A
    D'Souza, I
    Lee, VMY
    Reed, L
    Trojanowski, JQ
    Zhukareva, V
    Bird, T
    Schellenberg, G
    Wilhelmsen, KC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) : 13103 - 13107
  • [8] Djarmati Ana, 2004, Hum Mutat, V23, P525, DOI 10.1002/humu.9240
  • [9] Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD
    Eerola, J
    Hernandez, D
    Launes, J
    Hellström, O
    Hague, S
    Gulick, C
    Johnson, J
    Peuralinna, T
    Hardy, J
    Tienari, PJ
    Singleton, AB
    [J]. NEUROLOGY, 2003, 61 (07) : 1000 - 1002
  • [10] Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation
    Hague, S
    Rogaeva, E
    Hernandez, D
    Gulick, C
    Singleton, A
    Hanson, M
    Johnson, J
    Weiser, R
    Gallardo, M
    Ravina, B
    Gwinn-Hardy, K
    Crawley, A
    St George-Hyslop, PH
    Lang, AE
    Heutink, P
    Bonifati, V
    Hardy, J
    Singleton, A
    [J]. ANNALS OF NEUROLOGY, 2003, 54 (02) : 271 - 274