ⓘ Congenital amegakaryocytic thrombocytopenia

                                     

ⓘ Congenital amegakaryocytic thrombocytopenia

The primary manifestations are thrombocytopenia and megakaryocytopenia, or low numbers of platelets and megakaryocytes. There is an absence of megakaryocytes in the bone marrow with no associated physical abnormalities.

                                     
  • dominant thrombocytopenia Bernard Soulier syndrome associated with large platelets Congenital amegakaryocytic thrombocytopenia Congenital amegakaryocytic thrombocytopenia
  • platelet levels. Congenital amegakaryocytic thrombocytopenia CAMT is a rare inherited disorder. The primary manifestations are thrombocytopenia and megakaryocytopenia
  • refer to: Center for Arts Management and Technology Congenital Amegakaryocytic Thrombocytopenia Commission on Accreditation of Medical Transport Systems
  • abnormal megakaryocytes. Cluster of differentiation Congenital amegakaryocytic thrombocytopenia GRCh38: Ensembl release 89: ENSG00000117400 - Ensembl
  • constitutional macro thrombocytopenia ACMT In 2005, to avoid confusion between ACMT and congenital amegakaryocytic thrombocytopenia CAMT this CAMT entity
  • a 50 chance of having the condition. When associated with amegakaryocytic thrombocytopenia this inheritance has been found to be caused by mutations to
  • hemorrhage ATRUS Syndrome Thrombocytopenia 2 THC2 Congenital amegakaryocytic thrombocytopenia TAR syndrome Familial platelet disorder with predisposition