Evidence map›Paper›PMID 42130359›Full record

ArticleZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics2026

[Clinical analysis of six patients with pyruvate kinase deficiency caused by

Wen Wang, Yan-Xia Zhao, Ling-Zhen Wang, Fan Jiang, Jing Yang, Li-Rong Sun, Hui-Juan Xu

Abstract readEnglish Abstract
In one paragraph

Article in Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Wen WangDepartment of Pediatric Hematology and Oncology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, China.
Yan-Xia ZhaoDepartment of Pediatric Hematology and Oncology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, China.
Ling-Zhen WangDepartment of Pediatric Hematology and Oncology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, China.
Fan JiangDepartment of Pediatric Hematology and Oncology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, China.
Jing YangDepartment of Pediatric Hematology and Oncology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, China.
Li-Rong SunDepartment of Pediatric Hematology and Oncology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, China.
Hui-Juan XuDepartment of Pediatric Hematology and Oncology, Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the clinical features, treatment, and prognosis of pyruvate kinase deficiency (PKD) caused by

methodsClinical data of six patients with PKD who received care at the Affiliated Hospital of Qingdao University from August 2014 to August 2025 were retrospectively analyzed.

resultsOf the six patients, five were children with onset in infancy, and one was an adult whose disease onset occurred at school age. All presented with jaundice and anemia, and PKD was confirmed by genetic testing. Two patients underwent splenectomy due to frequent transfusion. Three patients were mild, required no regular transfusion, and did not undergo splenectomy. One patient died.

conclusionsPKD manifests chronic hemolysis with variable clinical severity. Genetic testing is recommended for diagnosis. Curative therapy remains lacking; management is mainly supportive. Splenectomy may reduce transfusion dependence and improve quality of life.

Indexed as

Anemia, Hemolytic, Congenital NonspherocyticPyruvate KinasePyruvate Metabolism, Inborn ErrorsAdolescentAdultChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesSplenectomyPKLR protein, humanPyruvate KinaseClinical featurePKLR gene variantPyruvate kinase deficiencySplenectomy

Identifiers

PMID42130359
PMCPMC13173477

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