Evidence map›Paper›PMID 40693691›Full record

ArticleEuropean journal of haematology2026

Interstitial 11q Deletions and Terminal 11q Duplications Cause a Bleeding Tendency due to Platelet Dysfunction That Is Similar to 11q Deletions Causing Jacobsen Syndrome.

Elise J Huisman, Virgil A S H Dalm, Marieke Joosten, Frans J Smiers, Leendert Porcelijn, Arjan Hoogendijk, Hans Janssen, Nicole N van der Wel, Idske C L Kremer Hovinga, Masja de Haas and 1 more

Abstract read
In one paragraph

Article in European journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Elise J HuismanDepartment of Pediatric Hematology and Oncology, Erasmus MC Sophia Children's Hospital, University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-0700-2194
Virgil A S H DalmDepartment of Internal Medicine, Division of Allergy and Clinical Immunology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0001-5945-4435
Marieke JoostenDepartment of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-4443-4690
Frans J SmiersDepartment of Pediatric Hematology, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, the Netherlands.ORCID https://orcid.org/0000-0002-8131-3521
Leendert PorcelijnLaboratory of Immunohematology Diagnostics, Sanquin Diagnostic Services, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0001-9441-0446
Arjan HoogendijkDepartment of Proteomics and Cell Biology, Sanquin Research, Amsterdam, the Netherlands.
Hans JanssenDepartment of Electron Microscopy, Dutch Cancer Institute - NKI, Amsterdam, the Netherlands.
Nicole N van der WelDepartment of Electron Microscopy, Amsterdam University Medical Center, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0001-6392-3417
Idske C L Kremer HovingaDepartment of Pediatric Hematology, Center for Benign Hematology, Thrombosis and Haemostasis, Van Creveldkliniek, University Medical Center Utrecht, Utrecht University, the Netherlands.ORCID https://orcid.org/0000-0002-6244-0429
Masja de HaasUnit of Transfusion Medicine, Sanquin Blood Supply, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0002-7044-0525
Marjon H CnossenDepartment of Pediatric Hematology and Oncology, Erasmus MC Sophia Children's Hospital, University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0003-1557-2995

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionJacobsen syndrome, resulting from a terminal deletion of chromosome 11 (11q), may lead to an increased bleeding tendency due to low platelet counts or platelet dysfunction. Currently, information on bleeding tendency and platelet function in patients with nonterminal 11q-aberrations such as larger deletions, interstitial 11q-deletions, or 11q-duplications is lacking.

methodsWe investigated the bleeding symptoms in relation to platelet numbers and function in 14 patients: 10 patients with a terminal 11q-deletion, one terminal 11q-duplication, two interstitial 11q-deletions, and one with an interstitial 11q-duplication.

resultsTwelve patients reported bleeding complications (12/14, 86%), most frequently perioperative bleeding (21%), hematomas (17%), epistaxis (13%), prolonged bleeding, and severe bruising (11%) and heavy menstrual bleeding in 4/5 postmenarcheal women (80%). Seven (50%) had platelet counts below normal values (median 62 × 10

conclusionsWe demonstrated increased bleeding tendency due to platelet disorders in the majority of patients with terminal 11q-deletions but also in nonterminal 11q-aberrations. This is confirmed by abnormal platelet function tests and MS. We therefore recommend screening of patients with all forms of 11q-disorders and, when indicated, preventive preoperative measurements and counseling for heavy menstrual bleeding in females.

Indexed as

Blood Platelet DisordersBlood PlateletsChromosome DeletionChromosomes, Human, Pair 11HemorrhageJacobsen Distal 11q Deletion SyndromeAdolescentAdultChildFemaleHumansMaleMiddle AgedPlatelet CountPlatelet Function TestsYoung Adultblood coagulation disorders [MESH]blood platelet disorders [MESH]chromosome 11qelectron [MESH]Jacobsen distal 11q deletion syndrome [MESH]mass‐spectrometry [MESH]microscopyplatelet granule deficiency disorder [MESH]trisomy [MESH]

Identifiers

PMID40693691
PMCPMC13460841

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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.