Management of neonatal purpura fulminans with severe protein C deficiency.
Indian Pediatr
;
2006 Jun; 43(6): 542-5
Article
Dans Anglais
| IMSEAR
| ID: sea-13124
ABSTRACT
Neonatal purpura fulminans is a life threatening clinical entity characterized by extensive subcutaneous thrombosis and disseminated intravascular coagulation usually manifesting shortly after birth. We report an autosomal recessive form of the disease in a neonate who was diagnosed with compound heterozygosity for mutations in his protein C gene as the molecular basis of his disorder.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
/
Humains
/
Mâle
/
Nouveau-né
/
Protéine C
/
Appréciation des risques
/
Thrombophilie
/
Déficit en protéine C
/
Anticoagulants
/
Mutation
Type d'étude:
Etude d'étiologie
/
Facteurs de risque
langue:
Anglais
Texte intégral:
Indian Pediatr
Année:
2006
Type:
Article
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