Results 21 to 30 of about 511,787 (144)

A hemizygous p.R204Q mutation in the ALAS2 gene underlies X-linked sideroblastic anemia in an adult Chinese Han man

open access: yesBMC Medical Genomics, 2021
Background X-linked sideroblastic anemia (XLSA) is the most common form of congenital sideroblastic anemia (CSA), and is associated with the mutations in the 5-aminolevulinate synthase 2 (ALAS2).
Jinbo Huang   +9 more
doaj   +1 more source

Acquired Sideroblastic Anemia: An Exploratory Comparative Statistical Analysis Between Clonal and Non-clonal Cases [PDF]

open access: yes, 2022
Sideroblastic anemia (SA) is a rare heterogenous group of inherited and acquired bone marrow disorders. We retrospectively studied the clinicopathologic characteristics, cytogenetic findings, and disease outcome of patients with acquired sideroblastic ...
Soliman, Dina S.   +17 more
core   +1 more source

A rare case of isoniazid induced sideroblastic anemia [PDF]

open access: yes, 2023
Sideroblastic anemia is a rare cause of anemia. Most of it accounts for the genetic cause, while drug induced is still uncommon. Our patient, a 20 year old female, is a known case of right frontal tuberculoma on ATT presented with complaints of ...
Gulati, Shipra   +3 more
core   +1 more source

Causes and Pathophysiology of Acquired Sideroblastic Anemia

open access: yes, 2022
The sideroblastic anemias are a heterogeneous group of inherited and acquired disorders characterized by anemia and the presence of ring sideroblasts in the bone marrow.
Leonor Arenillas   +6 more
core   +1 more source

Exploring the mechanistic link between SF3B1 mutation and ring sideroblast formation in myelodysplastic syndrome

open access: yesScientific Reports, 2022
Acquired sideroblastic anemia, characterized by bone marrow ring sideroblasts (RS), is predominantly associated with myelodysplastic syndrome (MDS). Although somatic mutations in splicing factor 3b subunit 1 (SF3B1), which is involved in the RNA splicing
Tetsuro Ochi   +13 more
doaj   +1 more source

Identification of a novel erythroid-specific enhancer for the ALAS2 gene and its loss-of-function mutation which is associated with congenital sideroblastic anemia

open access: yesHaematologica, 2014
Erythroid-specific 5-aminolevulinate synthase (ALAS2) is the rate-limiting enzyme for heme biosynthesis in erythroid cells, and a missense mutation of the ALAS2 gene is associated with congenital sideroblastic anemia.
Kiriko Kaneko   +6 more
doaj   +1 more source

COVID-19 associated respiratory failure complicating a pericardial effusion in a patient with sideroblastic anemia

open access: yesRespiratory Medicine Case Reports, 2021
Background: COVID-19 disease has been associated with several cardiovascular complications that rarely occur in the acute phase of the disease. Case report: A 13-year-old pediatric patient with congenital sideroblastic anemia associated with YARS2 ...
Edouard Sayad   +5 more
doaj   +1 more source

Iron metabolism in erythroid cells and patients with congenital sideroblastic anemia [PDF]

open access: yesInternational Journal of Hematology, 2017
Sideroblastic anemias are anemic disorders characterized by the presence of ring sideroblasts in a patient's bone marrow. These disorders are typically divided into two types, congenital or acquired sideroblastic anemia. Recently, several genes were reported as responsible for congenital sideroblastic anemia; however, the relationship between the ...
Kazumichi Furuyama, Kiriko Kaneko
openaire   +2 more sources

X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations [PDF]

open access: yes, 2014
X-linked sideroblastic anemia (XLSA) is the most common form of congenital sideroblastic anemia. In affected males, it is uniformly associated with partial loss-of-function missense mutations in the erythroid-specific heme biosynthesis protein 5 ...
van Wijk, Richard   +78 more
core   +1 more source

Sideroblastic anemia [PDF]

open access: yes, 2016
Sideroblastic anemias are a heterogenous group of disorders that have as a common feature with the presence of ringed sideroblasts in the marrow. We present a case of young female, nursing student who presented with increasing palpitation, fatigue and ...
A Shrestha, P Bhandari, R Hamal
core   +1 more source

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