Thrombocytopenia, acquired amegakaryocytic

Common Name(s)

Thrombocytopenia, acquired amegakaryocytic

Acquired amegakaryocytic thrombocytopenia is characterized by severe thrombocytopenia (lack of platelets) with no other blood abnormalities. It is so named because the level of the large bone marrow cells that produce platelets, called megakaryocytes, are significantly lower or absent. The course of the condition is variable, but the condition can become life-threatening. Its cause is currently unknown.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Thrombocytopenia, acquired amegakaryocytic" for support, advocacy or research.

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Scientific Literature

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The terms "Thrombocytopenia, acquired amegakaryocytic" returned 0 free, full-text review articles on human participants.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

CD34+ (Non-Malignant) Stem Cell Selection for Patients Receiving Allogeneic Stem Cell Transplantation
 

Status: Recruiting

Condition Summary: Bone Marrow Failure Syndrome; Severe Aplastic Anemia; Severe Congenital Neutropenia; Amegakaryocytic Thrombocytopenia; Diamond-Blackfan Anemia; Schwachman Diamond Syndrome; Primary Immunodeficiency Syndromes; Acquired Immunodeficiency Syndromes; Histiocytic Syndrome; Familial Hemophagocytic Lymphocytosis; Lymphohistiocytosis; Macrophage Activation Syndrome; Langerhans Cell Histiocytosis (LCH); Hemoglobinopathies; Sickle Cell Disease; Sickle Cell-beta-thalassemia

 

Last Updated: 13 Jul 2017

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