[Alexander's disease].

Abstract excerpt

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.

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Child
• Share to Genetic Variation
• Share to Heterozygote