A Case of Congenital Hypoprothrombinemia
Journal of the Korean Pediatric Society
;
: 422-428, 1994.
Article
Dans Coréen
| WPRIM
| ID: wpr-37482
ABSTRACT
Congenital hypoprothrombinemia is a rare congenital coagulation defect. The clinical signs are manifestation of generalized tendency such as; mucosal bleeding, hypermenorrhea and post tooth extraction hemorrage. It is associated with prolongation of PT and PTT with normal thrombin time and decreased serum prothrombin level. A case with congenital hypoprothrombinemia was experienced by the authors. A 36 days old male baby was admitted with palor skin and vomiting started one day before admission. Right side brain parenchymal hemorrhage and left shift of lateral ventricle were on brain CT scan. Prologation of prothrombin time and partial prothrombin time with decreased serum prothrombin level were resulted. Serum factor I, V, VII, VIII, IX and X were within normal level. We report a case congenital hypoprothrombinemia with a brief review of relaed literatures.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Temps de prothrombine
/
Peau
/
Temps de thrombine
/
Extraction dentaire
/
Vomissement
/
Encéphale
/
Fibrinogène
/
Prothrombine
/
Tomodensitométrie
/
Ventricules latéraux
Limites du sujet:
Femelle
/
Humains
/
Mâle
langue:
Coréen
Texte intégral:
Journal of the Korean Pediatric Society
Année:
1994
Type:
Article
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