Alexander disease, or hypoproconvertinemia is a rare autosomic recessive coagulation disorder. The features include familial and/or personal history of bleeding, with an abnormal prothrombin period and a normal activated partial thromboplastin period. Coagulation and genetic studies allow subclassification with prognosis incidence for this disease. The authors report on a case of one family with Alexander disease.
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Auckland City Hosp, Neurol Dept, Auckland, New ZealandAuckland City Hosp, Neurol Dept, Auckland, New Zealand
Anderson, Neil E.
Alexander, Hamish S.
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Royal Brisbane & Womens Hosp, Kenneth G Jamieson Neurosurg Dept, Brisbane, Qld, Australia
Univ Queensland, Fac Med, Brisbane, Qld, AustraliaAuckland City Hosp, Neurol Dept, Auckland, New Zealand
Alexander, Hamish S.
Messing, Albee
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Univ Wisconsin Madison, Waisman Ctr, Dept Comparat Biosci, Madison, WI USAAuckland City Hosp, Neurol Dept, Auckland, New Zealand