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Congenital amegakaryocytic thrombocytopenia (CAMT): a case report with review of literature.
Indian J Pathol Microbiol ; 2007 Jul; 50(3): 659-60
Article in English | 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.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Thrombocytopenia / Female / Humans / Male / Megakaryocytes / Child / Adult Type of study: Prognostic study Language: English Journal: Indian J Pathol Microbiol Year: 2007 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Thrombocytopenia / Female / Humans / Male / Megakaryocytes / Child / Adult Type of study: Prognostic study Language: English Journal: Indian J Pathol Microbiol Year: 2007 Type: Article