Sideroblastic anemia acquired

Common Name(s)

Sideroblastic anemia acquired

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Sideroblastic anemia acquired" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Sideroblastic anemia acquired" returned 7 free, full-text research articles on human participants. First 3 results:

Heteroplasmic point mutations of mitochondrial DNA affecting subunit I of cytochrome c oxidase in two patients with acquired idiopathic sideroblastic anemia.
 

Author(s): N Gattermann, S Retzlaff, Y L Wang, G Hofhaus, J Heinisch, C Aul, W Schneider

Journal: Blood. 1997 Dec;90(12):4961-72.

 

Mitochondrial iron overload in acquired idiopathic sideroblastic anemia (AISA) may be attributable to mutations of mitochondrial DNA (mtDNA), because these can cause respiratory chain dysfunction, thereby impairing reduction of ferric iron (Fe3+) to ferrous iron (Fe2+). The reduced ...

Last Updated: 29 Dec 1997

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Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid delta-aminolevulinate synthase (ALAS2) gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts.
 

Author(s): P D Cotter, A May, E J Fitzsimons, T Houston, B E Woodcock, A I al-Sabah, L Wong, D F Bishop

Journal: J. Clin. Invest.. 1995 Oct;96(4):2090-6.

 

X-linked sideroblastic anemia (XLSA) is caused by mutations of the erythroid-specific delta-aminolevulinate synthase gene (ALAS2) resulting in deficient heme synthesis. The characteristic hypochromic, microcytic anemia typically becomes manifest in the first three decades of life. ...

Last Updated: 13 Nov 1995

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Cytogenetic and cytochemical studies on progenitor cells of primary acquired sideroblastic anemia (PASA): involvement of multipotent myeloid stem cells in PASA clone and mosaicism with normal clone.
 

Author(s): T Amenomori, M Tomonaga, I Jinnai, H Soda, H Nonaka, T Matsuo, Y Yoshida, K Kuriyama, M Ichimaru, T Suematsu

Journal: Blood. 1987 Nov;70(5):1367-72.

 

By cytogenetic and cytochemical analyses of individual hematopoietic colonies, we investigated clonality in progenitor compartments of primary acquired sideroblastic anemia (PASA). Two of our four subjects had reduced but countable numbers of CFU-E, BFU-E, and GFU-GM in methylcellulose ...

Last Updated: 11 Dec 1987

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Reviews from the PubMed Database

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

 
 
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Symptoms, Diagnosis, and Treatment

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