Hemophilia a and congenital Hypofibrinogenemia: A rare association in same family.
Indian J Pediatr
;
2010 Feb; 77(2): 206-207
Artículo
en Inglés
| IMSEAR
| ID: sea-142504
ABSTRACT
Hemophilia A is the commonest inherited coagulation defect in human beings, whereas congenital hypofibrinogenemia is a much rarer disease. Occurrence of these two inherited diseases in the same family has not been reported so far. Younger sibling of a known case of Hemophilia A presented with recurrent, spontaneously occurring echymotic spots having prolonged PT, APTT, TT and very low absolute fibrinogen level with normal factor VIII level ultimately diagnosed as a case of congenital hypofibrinogenemia.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Humanos
/
Masculino
/
Fibrinógeno
/
Preescolar
/
Hemofilia A
Idioma:
Inglés
Revista:
Indian J Pediatr
Año:
2010
Tipo del documento:
Artículo
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