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Indian J Pathol Microbiol ; 2007 Jul; 50(3): 659-60
Artículo en Inglés | IMSEAR | ID: sea-74233

RESUMEN

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.


Asunto(s)
Adulto , Niño , Femenino , Humanos , Masculino , Megacariocitos/citología , Trombocitopenia/congénito
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