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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
1992-5-20
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pubmed:abstractText |
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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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-3050
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
55
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
227-8
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pubmed:dateRevised |
2010-9-7
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pubmed:meshHeading |
pubmed-meshheading:1564489-Blood Coagulation Tests,
pubmed-meshheading:1564489-Brain Damage, Chronic,
pubmed-meshheading:1564489-Cerebral Hemorrhage,
pubmed-meshheading:1564489-Child,
pubmed-meshheading:1564489-Child, Preschool,
pubmed-meshheading:1564489-Consanguinity,
pubmed-meshheading:1564489-Factor V Deficiency,
pubmed-meshheading:1564489-Female,
pubmed-meshheading:1564489-Follow-Up Studies,
pubmed-meshheading:1564489-Humans,
pubmed-meshheading:1564489-Infant,
pubmed-meshheading:1564489-Male,
pubmed-meshheading:1564489-Neurologic Examination
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pubmed:year |
1992
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pubmed:articleTitle |
Familial intracranial haemorrhage due to factor V deficiency.
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pubmed:affiliation |
Department of Neurology and Pathology, Ruby Hall Clinic, Pune, India.
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pubmed:publicationType |
Journal Article,
Case Reports
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