Evidence map›Paper›PMID 39188287›Full record

ArticleFrontiers in genetics2024

Fahr's syndrome as the initial imaging characteristics of MELAS syndrome with a possible seizure activity and cardiac arrest: a case report.

Yan Zheng, Haohao Wu, Meng Zhang, Baogang Huang, Junsu Yang, Chuan Liu, Hanmin Wang, Kang Du

Abstract readCase Reports
In one paragraph

Article in Frontiers in genetics, 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
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

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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. Silent stone: Idiopathic presentation of Fahr's disease.SAGE open medical case reports · 2025
    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

8 authors.

Yan Zheng *Department of Neurology, Qujing First People's Hospital, Qujing, Yunnan, China.
Haohao Wu *Department of Neurology, Qujing First People's Hospital, Qujing, Yunnan, China.
Meng Zhang *Teaching and Research Office of Internal Medicine, Qujing Medical College, Qujing, Yunnan, China.
Baogang HuangDepartment of Neurology, Qujing First People's Hospital, Qujing, Yunnan, China.
Junsu YangDepartment of Neurology, Qujing First People's Hospital, Qujing, Yunnan, China.
Chuan LiuDepartment of Urology, Qujing First People's Hospital, Qujing, Yunnan, China.
Hanmin WangDepartment of Endocrinology and Metabolism, Qujing First People's Hospital, Qujing, Yunnan, China.
Kang DuDepartment of Neurology, Qujing First People's Hospital, Qujing, Yunnan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study reported a case of MELAS syndrome presenting as the initial imaging characteristics of Fahr's syndrome with "near" sudden unexpected death in epilepsy (SUDEP) and lateralized periodic discharges (LPD). The patient, a young boy, experienced loss of consciousness 2 days prior, which was followed by two limb and facial convulsions. He was later found in cardiac arrest during hospitalization, but regained consciousness gradually after receiving cardiopulmonary resuscitation and tracheal intubation. The patient exhibited short stature, intellectual disability, poor sports abilities, and academic performance since childhood, but had no family history. Emergency head computed tomography (CT) revealed high density calcification in bilateral caudate nucleus, lentiform nucleus, thalamus, and dentate nucleus with evidence of an acute process. The patient was transferred to the neurology department where he continued to recover consciousness, though he experienced dysarthria, left limb hemiplegia, and hemiparesthesia. Changes in head magnetic resonance imaging (MRI) findings were noted at admission, 1 month later, and 6 months later. LPD were observed in his video electroencephalogram. The CT urography indicated a narrow left ureteropelvic junction with left hydronephrosis, which was suggestive of ureteropelvic junction obstruction. Ultimately, a diagnosis of near-SUDEP was suspected in this patient, indicating a rare case of MELAS syndrome with near-SUDEP and LPD. The gene tests results revealed the presence of the mitochondrial DNA A3243G mutation, leading to the final diagnosis of MELAS syndrome. This case expands the clinical disease spectrum of the MELAS syndrome.

Indexed as

Fahr’s syndromeLPDMELAS syndromenear-SUDEPUPJO

Identifiers

PMID39188287
PMCPMC11345220

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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.