Congenital amegakaryocytic thrombocytopenia (CAMT): a case report with review of literature.
Indian J Pathol Microbiol
;
2007 Jul; 50(3): 659-60
Article
Dans Anglais
| IMSEAR
| ID: sea-74233
ABSTRACT
Congenital amegakaryocytic thrombocytopenia (CAMT) is an uncommon cause of thrombocytopenia in children. Mutations in the thrombopoietin (Tpo) receptor gene C-mpl were found to be the likely cause of thrombocytopenia and complete marrow failure. Two types are identified CAMT with or without congenital anomalies. We report a case of the latter type for its extreme rarity.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Thrombopénie
/
Femelle
/
Humains
/
Mâle
/
Mégacaryocytes
/
Enfant
/
Adulte
Type d'étude:
Étude pronostique
langue:
Anglais
Texte intégral:
Indian J Pathol Microbiol
Année:
2007
Type:
Article
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