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Article

[Familial platelet disorder with predisposition to myeloid leukemia (FPD/AML): a case report and literature review].

Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi - 14 Apr 2021

Zhang R R, Chen X J, Ren Y Y, Yang W Y, Zhu X F

Abstract excerpt

Objective: To analyze the clinical features, bone marrow features, and gene mutations of children with familial platelet disorder with predisposition to myeloid leukemia (FPD/AML) caused by a RUNX1 germline mutation as well as their family members. Methods: The clinical data and gene mutations of a child with FPD/AML hospitalized in the Pediatric Blood Disease Center, Institute of Hematology and Blood Diseases...

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Share to Blood Coagulation Disorders, Inherited
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 33979975
DOI: 10.3760/cma.j.issn.0253-2727.2021.04.007
PMCID: PMC8120121

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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