FAMILIAL INTRACRANIAL HEMORRHAGE DUE TO FACTOR-V DEFICIENCY

被引:3
|
作者
WADIA, RS [1 ]
SANGLE, SA [1 ]
KRIPALANEY, S [1 ]
BAFNA, M [1 ]
KARVE, SR [1 ]
机构
[1] SASSOON HOSP, DEPT GENET & NEUROL, POONA, INDIA
来源
关键词
D O I
10.1136/jnnp.55.3.227
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Strokes may occur with a large number of genetic disorders. Natowicz and Kelley have reviewed the single gene disorders capable of causing familial haemorrhagic strokes. These may be classified into four groups: a) hereditary disorders affecting clotting factors or platelets; b) hereditary disease producing vascular anomaly; c) hereditary disease causing hypertension and d) miscellaneous group including neurofibromatosis, sickle cell disease and tuberous sclerosis.
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页码:227 / 228
页数:2
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