Thiamine-Responsive Megaloblastic Anemia Syndrome Mimicking Myelodysplastic Neoplasm

Late-onset TRMA should be considered in adult patients with indicative comorbidities and a typical phenotype, which may mimic features of MDS.

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Publication Details

Journal
Acta Haematologica
Published
2024-10-28
DOI
https://doi.org/10.1159/000542286
Citations
1
Primary Topic
Folate and B Vitamins Research
Type
article
Field-Weighted Citation Impact
0.47
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article

Thiamine-Responsive Megaloblastic Anemia Syndrome Mimicking Myelodysplastic Neoplasm

H. Faust, Klaus Hans Metzeler, Henry Oppermann, Anne Sophie Kubasch et al.
1 citations
Acta Haematologica
Folate and B Vitamins Research
0.47
article

Thiamine-Responsive Megaloblastic Anemia Syndrome Mimicking Myelodysplastic Neoplasm

H. Faust, Klaus Hans Metzeler, Henry Oppermann, Anne Sophie Kubasch, Jens Uhlig, Vladan Vučinić, Robin‐Tobias Jauss, Denny Popp, Johannes R. Lemke, Freya Schnabel, Madlen Jentzsch, Uwe Platzbecker, Christina Klötzer, Georg‐Nikolaus Franke
article en
1 citations

Abstract

Late-onset TRMA should be considered in adult patients with indicative comorbidities and a typical phenotype, which may mimic features of MDS.

Acta HaematologicaVol. 148(4)
University Hospital Leipzig (DE), Orthopädische Praxis (DE), Leipzig University (DE)
Good health and well-being
Openalex Percentile: Top 30%
Folate and B Vitamins Research
0.47
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