Evidence map›Paper›PMID 40257477›Full record

ArticleAnnals of hematology2025

From severe aplastic anemia with TERT variant to Wilson disease - associations or not.

Tong Chen, Jia Song, Limin Xing, Jin Chen, Xifeng Dong, Lijuan Li, Junfeng Yang, Wentian Liu, Zonghong Shao, Rong Fu

Abstract readCase Reports
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Tong Chen *Department of Hematology, Tianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin Medical University General Hospital, Tianjin, China.
Jia Song *Department of Hematology, Tianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin Medical University General Hospital, Tianjin, China.
Limin XingDepartment of Hematology, Tianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin Medical University General Hospital, Tianjin, China.
Jin ChenDepartment of Hematology, Tianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin Medical University General Hospital, Tianjin, China.
Xifeng DongDepartment of Hematology, Tianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin Medical University General Hospital, Tianjin, China.
Lijuan LiDepartment of Hematology, Tianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin Medical University General Hospital, Tianjin, China.
Junfeng YangDepartment of Neurology, Institute of Neurology, Tianjin Medical University General Hospital, Tianjin, China.
Wentian LiuDepartment of Gastroenterology, Tianjin Medical University General Hospital, Tianjin Institute of Digestive Disease, Tianjin, China.
Zonghong ShaoDepartment of Hematology, Tianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin Medical University General Hospital, Tianjin, China.
Rong FuDepartment of Hematology, Tianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin Medical University General Hospital, Tianjin, China. furong8369@tmu.edu.cn.ORCID http://orcid.org/0000-0002-9928-9224

Funding

National Natural Science Foundation of China 81900125National Natural Science Foundation of China 81970115Natural Science Foundation of Tianjin Municipality 20JCQNJC00570Tianjin Key Medical Discipline (Specialty) Construction project TJYXZDXK-028A
6 · The paper itself

Abstract

Severe aplastic anemia is a life-threatening ineffective hematopoiesis, arising from inherited or acquired traits. Wilson disease is a rare congenital metabolic disorder with copper accumulation. Here we report a rare case of a 15-year-old boy, who presented with bone marrow failure. Whole exome sequencing revealed several gene mutations in ATP7B and TERT. Based on the phenotypes, telomere lengths and pedigree of his family, the patient was diagnosed with severe aplastic anemia accompanied by Wilson disease. Allogeneic hematopoietic stem cell transplantation and anti-copper therapy helped him achieve transfusion independence and restore relatively normal copper metabolism. We discussed the possible associations between the two rare conditions and optimal management in this situation.

Indexed as

Anemia, AplasticHepatolenticular DegenerationMutationTelomeraseAdolescentCopperCopper-Transporting ATPasesHematopoietic Stem Cell TransplantationHumansMalePedigreeATP7B protein, humanCopperCopper-Transporting ATPasesTelomeraseTERT protein, humanAplastic anemiaHematopoietic stem cell transplantationShort telomere syndromeTelomere lengthWilson disease

Identifiers

PMID40257477
PMCPMC12141154

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.