Article
[Alexander's disease].
Pediatrie - 1 Jan 1991
Elian J C, Frappaz D, Reynaud J, Perrot S, Freycon F
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 subclas...
Topics
- Child
- Factor VII Deficiency
- Genetic Variation
- Heterozygote
- Homozygote
- Humans
- Male
