Evidence map›Paper›PMID 41721658›Full record

ArticleJournal of investigative medicine high impact case reports

A Case Report of Thrombocytopenia Caused by a May-Hegglin Anomaly in a Young Saudi Female.

Rehab Y Al-Ansari, Rawan Rashed Aljohani, Rayan Mansour Aljurbua, Ali Mohammed Alasmari, Muhammad F Abdellatif, Nawaf Zakary

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of investigative medicine high impact case reports. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

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

6 authors.

Rehab Y Al-AnsariInternal Medicine Department, KFMMC, Dhahran, Kingdom of Saudi Arabia.ORCID 0000-0003-4331-5769
Rawan Rashed AljohaniInternal Medicine Department, KFMMC, Dhahran, Kingdom of Saudi Arabia.
Rayan Mansour AljurbuaInternal Medicine Department, KFMMC, Dhahran, Kingdom of Saudi Arabia.
Ali Mohammed AlasmariLaboratory Department, KFMMC, Dhahran, Kingdom of Saudi Arabia.
Muhammad F AbdellatifInternal Medicine Department, KFMMC, Dhahran, Kingdom of Saudi Arabia.
Nawaf ZakaryInternal Medicine Department, KFMMC, Dhahran, Kingdom of Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low platelet count is rarely caused by inherited thrombocytopenia. May-Hegglin anomaly is an uncommon condition that falls under the umbrella of familial thrombocytopenia. The condition is under-reported in Saudi Arabia; therefore, we report the current case. This is a 24-year-old Saudi lady, presented to the emergency room with vaginal bleeding. No bleeding occurred at any other sites. She has a positive family history of thrombocytopenia among her father and 2 of her siblings. Her platelet count was 16 × 10

Indexed as

Hearing Loss, SensorineuralMolecular Motor ProteinsMyosin Heavy ChainsThrombocytopeniaFemaleHumansMutationPlatelet CountSaudi ArabiaYoung AdultMolecular Motor ProteinsMYH9 protein, humanMyosin Heavy Chainsgene mutationinheritedMay–Hegglin anomalyMYH9thrombocytopenia

Identifiers

PMID41721658
PMCPMC12924981

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Registered trials

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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.