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铁粒幼细胞性贫血

Sideroblastic anemia

ORPHA:1047疾病组

定义 英文原文(暂无中文)

Sideroblastic anemias (SA) are a group of rare heterogeneous inherited or acquired bone marrow disorders, isolated or part of a syndrome, characterized by decreased hemoglobin synthesis, because of defective use of iron (although plasmatic iron levels may be normal or elevated) and the presence of ringed sideroblasts in the bone marrow due to the pathologic iron overload in mitochondria as visualized by Perls' staining. The group encompasses (idiopathic) acquired sideroblastic anemia and constitutional sideroblastic anemias. The latter include syndromic sideroblastic anemias such as Pearson syndrome, mitochondrial mypathy and sideroblastic anemias, x-linked sideroblastic anemia-ataxia, thiamine responsive megaloblastic anemia syndrome and nonsyndromic sideroblastic anemias comprising x-linked and autosomal recessive sideroblastic anemias.

基本事实

遗传方式
常染色体显性、常染色体隐性、线粒体遗传、不适用、X 连锁显性、X 连锁隐性
发病年龄
各年龄段

相关基因 11来自下位疾病

Orphanet 未在本条目上直接标注致病基因。下表由本组所属的下位疾病汇总而来,「来源条目」列给出基因实际标注在哪一个 ORPHA 条目上。

基因名称来源条目
ABCB7ATP binding cassette subfamily B member 7ORPHA:2802
ALAS25'-aminolevulinate synthase 2ORPHA:75563
GLRX5glutaredoxin 5ORPHA:255132
HSPA9heat shock protein family A (Hsp70) member 9ORPHA:260305
PUS1pseudouridine synthase 1ORPHA:2598
SF3B1splicing factor 3b subunit 1ORPHA:75564
SLC25A38solute carrier family 25 member 38ORPHA:260305
STEAP3STEAP3 metalloreductaseORPHA:300298
TET2tet methylcytosine dioxygenase 2ORPHA:75564
TRNT1tRNA nucleotidyl transferase 1ORPHA:369861
YARS2tyrosyl-tRNA synthetase 2ORPHA:2598

外部标识与链接

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本页数据来源

  • 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
  • 中文病名:Orphanet 中文包,冻结于 2020-06-01
  • 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)