Evidence map›Paper›PMID 37438874›Full record

ArticleNeuropathology : official journal of the Japanese Society of Neuropathology2024

Multisystem pathology in McLeod syndrome.

Katherine R Schon, Dominic G O'Donovan, Mayen Briggs, James B Rowe, Lokesh Wijesekera, Patrick F Chinnery, Jelle van den Ameele

Open access · hybridAbstract readCase Reports
In one paragraph

Article in Neuropathology : official journal of the Japanese Society of Neuropathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 35% of its field
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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

7 authors at 2 institutions in 1 country.

Katherine R SchonDepartment of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK.ORCID https://orcid.org/0000-0001-8054-8954
Dominic G O'DonovanDepartment of Pathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Mayen BriggsDepartment of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK.
James B RoweDepartment of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK.
Lokesh WijesekeraDepartment of Clinical Neurophysiology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Patrick F ChinneryDepartment of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK.
Jelle van den AmeeleDepartment of Clinical Neurosciences, School of Clinical Medicine, University of Cambridge, Cambridge, UK.ORCID https://orcid.org/0000-0002-2744-0810
University of Cambridge · GBCambridge University Hospitals NHS Foundation Trust · GB

Funding

Medical Research Council MC_UU_00028/7Medical Research Council MC_UU_00028/8Wellcome Trust
6 · The paper itself

Abstract

We present a comprehensive characterization of clinical, neuropathological, and multisystem features of a man with genetically confirmed McLeod neuroacanthocytosis syndrome, including video and autopsy findings. A 61-year-old man presented with a movement disorder and behavioral change. Examination showed dystonic choreiform movements in all four limbs, reduced deep-tendon reflexes, and wide-based gait. He had oromandibular dyskinesia causing severe dysphagia. Elevated serum creatinine kinase (CK) was first noted in his thirties, but investigations, including muscle biopsy at that time, were inconclusive. Brain magnetic resonance imaging showed white matter volume loss, atrophic basal ganglia, and chronic small vessel ischemia. Despite raised CK, electromyography did not show myopathic changes. Exome gene panel testing was negative, but targeted genetic analysis revealed a hemizygous pathogenic variant in the XK gene c.895C > T p.(Gln299Ter), consistent with a diagnosis of McLeod syndrome. The patient died of sepsis, and autopsy showed astrocytic gliosis and atrophy of the basal ganglia, diffuse iron deposition in the putamen, and mild Alzheimer's pathology. Muscle pathology was indicative of mild chronic neurogenic atrophy without overt myopathic features. He had non-specific cardiomyopathy and splenomegaly. McLeod syndrome is an ultra-rare neurodegenerative disorder caused by X-linked recessive mutations in the XK gene. Diagnosis has management implications since patients are at risk of severe transfusion reactions and cardiac complications. When a clinical diagnosis is suspected, candidate genes should be interrogated rather than solely relying on exome panels.

Indexed as

Muscular DiseasesNeuroacanthocytosisAtrophyBasal GangliaHumansMaleMiddle AgedautopsyMcLeod syndromeraised CKXK gene

Identifiers

PMID37438874
PMCPMC7619572
OpenAlexW4384126664

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.