Discrepancy in factor VIII 1-stage/2-stage activity in a child with Arg(531)--> His mutation.
Blood Coagul Fibrinolysis
; 21(5): 474-5, 2010 Jul.
Article
em En
| MEDLINE
| ID: mdl-20614574
Routine screening of infants born to known hemophilia carriers includes a factor VIII (FVIII) level. In routine practice, mild FVIII deficiency variants may be missed by laboratories that exclusively use a one-stage activated partial thromboplastin time-based activity assay. This case illustrates such a possibility with a discrepancy between the one-stage and two-stage assays performed on a child who carries the Arg(531) --> His mutation.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Arginina
/
Fator VIII
/
Mutação de Sentido Incorreto
/
Hemofilia A
/
Histidina
Tipo de estudo:
Diagnostic_studies
Limite:
Child
/
Humans
/
Male
Idioma:
En
Revista:
Blood Coagul Fibrinolysis
Assunto da revista:
ANGIOLOGIA
/
HEMATOLOGIA
Ano de publicação:
2010
Tipo de documento:
Article
País de afiliação:
Austrália