Evidence map›Paper›PMID 37985634›Full record

ReviewNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2024

A chorea-acanthocytosis patient with novel mutations in the VPS13A gene without acanthocyte.

Shan Jin, Zhengzhe Sun, Xiang Fang, Huaizhen Chen, Wenming Yang, Shan Wang, Jinwei Fan

Abstract readCase ReportsReview
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In one paragraph

Review in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2024. 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, top 59% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Update on Genetic Chorea.Current neurology and neuroscience reports · 2026
    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.

Shan Jin *The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Shushan District, No.117, Meishan Road, Hefei, 230000, Anhui, China.
Zhengzhe Sun *Anhui University of Traditional Chinese Medicine, Hefei, Anhui, China.
Xiang FangThe First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Shushan District, No.117, Meishan Road, Hefei, 230000, Anhui, China. fxdxx@ahtcm.edu.cn.ORCID http://orcid.org/0000-0001-9716-8253
Huaizhen ChenThe First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Shushan District, No.117, Meishan Road, Hefei, 230000, Anhui, China.
Wenming YangThe First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Shushan District, No.117, Meishan Road, Hefei, 230000, Anhui, China.
Shan WangAnhui University of Traditional Chinese Medicine, Hefei, Anhui, China.
Jinwei FanAnhui University of Traditional Chinese Medicine, Hefei, Anhui, China.
Anhui University of Traditional Chinese Medicine · CNMinistry of Education of the People's Republic of China · CN

Funding

General program of Anhui Natural Science Foundation 2008085MH264General program of Anhui Natural Science Foundation 2208085MH271Key projects of natural science research in Colleges and universities in Anhui Province KJ2019A0457Scientific Research Fund of Anhui University of Traditional Chinese Medicine 2021yfylc10
6 · The paper itself

Abstract

Chorea-acanthocytosis (ChAc) is a rare clinical genetic disorder of the nervous system, which is characterized by choreiform movement disorder, cognitive decline, and psychiatric disorders. ChAc is mostly diagnosed based on its typical clinical manifestations and the increased number of acanthocytes in peripheral blood smears. Here, we report a patient, who has the characteristic clinical manifestations of ChAc with limb choreiform movements, involuntary lip and tongue bites, seizures, and emotional instability. However, her blood smear was negative for acanthocytes with scanning electron microscopy. We later identified two novel pathogenic mutations in the patient's vacuolar protein sorting homolog 13 A (VPS13A) on chromosome 9q21 by targeted gene sequencing, and she was definitively diagnosed with "ChAc." After treatment with carbamazepine, haloperidol, the patient's symptoms gradually improved. We consider that an acanthocyte negative blood smear cannot rule out ChAC diagnosis, and genetic testing is the "gold standard" for the diagnosis. Through a review of previous research, it is rare for a patient to have a clear diagnosis of ChAc by genetic testing, but whose blood smear is negative for acanthocytes with electron microscopy. In addition, in this report, we discovered two novel pathogenic mutations, which have not been reported previously, and extended the genetic characteristics of ChAc.

Indexed as

Movement DisordersNeuroacanthocytosisAcanthocytesFemaleHumansMutationVesicular Transport ProteinsVesicular Transport ProteinsVPS13A protein, humanChorea-acanthocytosisNovel pathogenic mutationTargeted gene sequencingVPS13A gene

Identifiers

PMID37985634
OpenAlexW4388840079

What OpenQuestion holds

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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.