Estimation of the gene frequency of aceruloplasminemia in Japan

被引:57
作者
Miyajima, H
Kohno, S
Takahashi, Y
Yonekawa, O
Kanno, T
机构
[1] Hamamatsu Univ Sch Med, Dept Med 1, Hamamatsu, Shizuoka 4313192, Japan
[2] Hamamatsu Univ Sch Med, Lab Med, Hamamatsu, Shizuoka 4313192, Japan
关键词
D O I
10.1212/WNL.53.3.617
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aceruloplasminemia is a newly recognized autosomal recessive disorder of iron metabolism that causes neurodegeneration of the retina and basal, ganglia as well as diabetes mellitus. We screened the serum ceruloplasmin concentrations of 4,990 healthy adult individuals. Subsequent sequence determination of the mutant alleles showed three mutations (5-bp insertion in exon 7, one heterozygote, one-bp deletion in exon 14, two heterozygotes, nonsense mutation in exon 15, one homozygote and two heterozygotes). The gene frequency was 70/100,000. In Japan, the incidence of aceruloplasminemia was estimated to be approximately 1 per 2,000,000 in the case of nonconsanguineous marriages.
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页码:617 / 619
页数:3
相关论文
共 10 条
[1]   A NONSENSE MUTATION OF THE CERULOPLASMIN GENE IN HEREDITARY CERULOPLASMIN DEFICIENCY WITH DIABETES-MELLITUS [J].
DAIMON, M ;
KATO, T ;
KAWANAMI, T ;
TOMINAGA, M ;
IGARASHI, M ;
YAMATANI, K ;
SASAKI, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 217 (01) :89-95
[2]   ACERULOPLASMINEMIA - MOLECULAR CHARACTERIZATION OF THIS DISORDER OF IRON-METABOLISM [J].
HARRIS, ZL ;
TAKAHASHI, Y ;
MIYAJIMA, H ;
SERIZAWA, M ;
MACGILLIVRAY, RTA ;
GITLIN, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) :2539-2543
[3]  
LOGAN JI, 1994, Q J MED, V87, P663
[4]   Use of desferrioxamine in the treatment of aceruloplasminemia [J].
Miyajima, H ;
Takahashi, Y ;
Kamata, T ;
Shimizu, H ;
Sakai, N ;
Gitlin, JD .
ANNALS OF NEUROLOGY, 1997, 41 (03) :404-407
[5]   FAMILIAL APOCERULOPLASMIN DEFICIENCY ASSOCIATED WITH BLEPHAROSPASM AND RETINAL DEGENERATION [J].
MIYAJIMA, H ;
NISHIMURA, Y ;
MIZOGUCHI, K ;
SAKAMOTO, M ;
SHIMIZU, T ;
HONDA, N .
NEUROLOGY, 1987, 37 (05) :761-767
[6]  
NEEL JV, 1949, AM J HUM GENET, V1, P156
[7]   Characterization of a nonsense mutation in the ceruloplasmin gene resulting in diabetes and neurodegenerative disease [J].
Takahashi, Y ;
Miyajima, H ;
Shirabe, S ;
Nagataki, S ;
Suenaga, A ;
Gitlin, JD .
HUMAN MOLECULAR GENETICS, 1996, 5 (01) :81-84
[8]   Effect of treatment of Wilson's disease on natural history of haemochromatosis [J].
Walshe, JM ;
Cox, DW .
LANCET, 1998, 352 (9122) :112-113
[9]   A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis [J].
Yazaki, M ;
Yoshida, K ;
Nakamura, A ;
Furihata, K ;
Yonekawa, M ;
Okabe, T ;
Yamashita, N ;
Ohta, M ;
Ikeda, S .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1998, 156 (01) :30-34
[10]   A MUTATION IN THE CERULOPLASMIN GENE IS ASSOCIATED WITH SYSTEMIC HEMOSIDEROSIS IN HUMANS [J].
YOSHIDA, K ;
FURIHATA, K ;
TAKEDA, S ;
NAKAMURA, A ;
YAMAMOTO, K ;
MORITA, H ;
HIYAMUTA, S ;
IKEDA, S ;
SHIMIZU, N ;
YANAGISAWA, N .
NATURE GENETICS, 1995, 9 (03) :267-272