Familial intracranial haemorrhage due to factor V deficiency.
AUTOR(ES)
Wadia, R S
RESUMO
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.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1014735Documentos Relacionados
- Intracerebral haemorrhage in an adult due to transient factor X deficiency
- Familial apolipoprotein E deficiency.
- Fetal anaemia due to pyruvate kinase deficiency.
- Factor V (Quebec): a bleeding diathesis associated with a qualitative platelet Factor V deficiency.
- Molecular basis for familial isolated growth hormone deficiency.