نتایج جستجو برای: sideroblastic anemia

تعداد نتایج: 56367  

Journal: :Blood 2007
Corinne Pondarre Dean R Campagna Brendan Antiochos Lindsay Sikorski Howard Mulhern Mark D Fleming

X-linked sideroblastic anemia with ataxia (XLSA/A) is a rare syndromic form of inherited sideroblastic anemia associated with spinocerebellar ataxia, and is due to mutations in the mitochondrial ATP-binding cassette transporter Abcb7. Here, we show that Abcb7 is essential for hematopoiesis and formally demonstrate that XLSA/A is due to partial loss of function mutations in Abcb7 that directly o...

Journal: :Blood 2003
Mario Cazzola Rosangela Invernizzi Gaetano Bergamaschi Sonia Levi Barbara Corsi Erica Travaglino Valeria Rolandi Giorgio Biasiotto Jim Drysdale Paolo Arosio

The sideroblastic anemias are characterized by ring sideroblasts, that is, red cell precursors with mitochondrial iron accumulation. We therefore studied the expression of mitochondrial ferritin (MtF) in these conditions. Erythroid cells from 13 patients with refractory anemia with ring sideroblasts (RARS) and 3 patients with X-linked sideroblastic anemia (XLSA) were analyzed for the distributi...

Journal: :Blood 1972
G F Riedler P W Straub

The dimorphic blood picture in sideroblastic anemia suggests the coexistence of at least two types of erythrocyte, the populations with the smaller RBCs being responsible for the crucial abnormality, namely the impairment of iron incorporation into protoporphyrin. In a patient with sideroblastic anemia who subsequently developed acute myelocytic leukemia, we found a light and a heavy cell popul...

Journal: :Blood 1977
R R Streeter C A Presant E Reinhard

In order to determine the prognostic significance of thrombocytosis in idiopathic sideroblastic anemia, the clinical courses of 17 patients were reviewed. Six patients (36%) had thrombocytosis, and none developed acute leukemia. Nine patients (53%) had normal platelet counts, and one developed acute leukemia. Two patients (12%) were thrombocytopenic, and one died of acute leukemia. There was li...

2005
Georg F. Riedler

The dimorphic blood picture in sideroblastic anemia suggests the coexistence of at least two types of erythrocyte, the populations with the smaller RBCs being responsible for the crucial abnormality, namely the impairment of iron incorporation into protoporphyrin. In a patient with sideroblastic anemia who subsequently developed acute myelocytic leukemia, we found a light and a heavy cell popul...

Journal: :Blood 2003
Kazumichi Furuyama Hideo Harigae Chiharu Kinoshita Toshihiko Shimada Kazuko Miyaoka Chiaki Kanda Yoshifumi Maruyama Shigeki Shibahara Shigeru Sassa

X-linked sideroblastic anemia (XLSA) is due to deficient activity of erythroid-specific 5-aminolevulinate synthase (ALAS2). We report here a patient who developed sideroblastic anemia at the age of 81 years while undergoing hemodialysis. The diagnosis of sideroblastic anemia was established by the presence of ringed sideroblasts in the bone marrow, and treatment with oral pyridoxine completely ...

Journal: :American Journal of Hematology 2011

Journal: :Haematologica 2011
Caroline Kannengiesser Mayka Sanchez Marion Sweeney Gilles Hetet Briedgeen Kerr Erica Moran Jose L Fuster Soler Karim Maloum Thomas Matthes Caroline Oudot Axelle Lascaux Corinne Pondarré Julian Sevilla Navarro Sudharma Vidyatilake Carole Beaumont Bernard Grandchamp Alison May

BACKGROUND Congenital sideroblastic anemias are rare disorders with several genetic causes; they are characterized by erythroblast mitochondrial iron overload, differ greatly in severity and some occur within a syndrome. The most common cause of non-syndromic, microcytic sideroblastic anemia is a defect in the X-linked 5-aminolevulinate synthase 2 gene but this is not always present. Recently, ...

Journal: :Haematologica 2004
Emília Cortesão Júlia Vidan Janet Pereira Paula Gonçalves Maria Letícia Ribeiro Gabriel Tamagnini

We report the case of a 40-year female who manifested late onset, pyridoxine-refractory X-linked sideroblastic anemia, heterozygous for the first described frameshift ALAS2 mutation, CD506-507 (-C). On presentation she had macrocytic anemia with severe iron overload.

Journal: :PLoS genetics 2016
J Pedro Fernández-Murray Sergey V Prykhozhij J Noelia Dufay Shelby L Steele Daniel Gaston Gheyath K Nasrallah Andrew J Coombs Robert S Liwski Conrad V Fernandez Jason N Berman Christopher R McMaster

Sideroblastic anemias are acquired or inherited anemias that result in a decreased ability to synthesize hemoglobin in red blood cells and result in the presence of iron deposits in the mitochondria of red blood cell precursors. A common subtype of congenital sideroblastic anemia is due to autosomal recessive mutations in the SLC25A38 gene. The current treatment for SLC25A38 congenital siderobl...

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