Sideroblastic anemia classification: Difference between revisions
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* Congenital | * Congenital | ||
* Acquired | * Acquired | ||
{| class="wikitable" | |||
|+ | |||
! colspan="2" |Congenital sideroblastic anaemias | |||
|- | |||
|X-linked | |||
|X-linked sideroblastic anaemia (XLSA) | |||
X-linked sideroblastic anaemia with ataxia (XLSA/A) | |||
|- | |||
|Autosomal | |||
|Glutaredoxin-5 deficiency | |||
Thiamine-responsive megaloblastic anaemia (TRMA) | |||
Associated with erythropoietic protoporphyria (EPP) | |||
Myopathy, lactic acidosis and sideroblastic anaemia (MLASA) | |||
|- | |||
|Mitochondrial DNA | |||
|Pearson syndrome | |||
|} | |||
==References== | ==References== |
Revision as of 14:43, 1 August 2018
Sideroblastic anemia Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Sideroblastic anemia classification On the Web |
American Roentgen Ray Society Images of Sideroblastic anemia classification |
Risk calculators and risk factors for Sideroblastic anemia classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Nazia Fuad M.D.
Overview
Classification
Sideroblastic anemia may be classified according to its etiology into two groups:
- Congenital
- Acquired
Congenital sideroblastic anaemias | |
---|---|
X-linked | X-linked sideroblastic anaemia (XLSA)
X-linked sideroblastic anaemia with ataxia (XLSA/A) |
Autosomal | Glutaredoxin-5 deficiency
Thiamine-responsive megaloblastic anaemia (TRMA) Associated with erythropoietic protoporphyria (EPP) Myopathy, lactic acidosis and sideroblastic anaemia (MLASA) |
Mitochondrial DNA | Pearson syndrome |