Incidence of hereditary bleeding disorders in Bradford, UK: variation with ethnic group

被引:5
作者
Macheta, MP [1 ]
Minford, AMB [1 ]
Parapia, LA [1 ]
机构
[1] BRADFORD ROYAL INFIRM,DEPT HAEMATOL,BRADFORD BD9 6RJ,W YORKSHIRE,ENGLAND
关键词
congenital platelet disorders; epidemiology; factor VII deficiency; factor XII deficiency; haemophilia;
D O I
10.1046/j.1365-2516.1997.00113.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have studied the number of patients registered with congenital bleeding disorders at the Haemophilia Centre, Bradford, UK, according to ethnic group. The large Pakistani population in Bradford presents a different spectrum of disorders compared with the indigenous Caucasian population with a significantly higher number of cases of factor VII deficiency and platelet disorders. Other haemophilia centres in the developed world serving large immigrant communities may also manage increased numbers of these rarer disorders with similar implications for resource allocation.
引用
收藏
页码:292 / 294
页数:3
相关论文
共 7 条
[1]  
AWIDI AS, 1984, THROMB HAEMOSTASIS, V51, P331
[2]   EHLERS-DANLOS SYNDROME, CLOTTING DISORDERS AND MUSCULAR-DYSTROPHY [J].
BERTIN, P ;
TREVES, R ;
JULIA, A ;
GAILLARD, S ;
DESPROGESGOTTERON, R .
ANNALS OF THE RHEUMATIC DISEASES, 1989, 48 (11) :953-956
[3]  
HALBMAYER WM, 1994, THROMB HAEMOSTASIS, V71, P68
[4]  
KHUNDURI U, 1981, THROMB HAEMOSTASIS, V45, P717
[5]  
LAMMLE B, 1991, THROMB HAEMOSTASIS, V65, P117
[6]  
MANNHALTER C, 1987, Fibrinolysis, V1, P259, DOI 10.1016/0268-9499(87)90046-4
[7]  
NATHWANI AC, 1992, EPIDEMIOLOGY HAEMA 2, P383