Evidence map›Paper›PMID 35624917›Full record

ArticleBrain sciences2022

Co-Occurrence of Multiple Sclerosis and Amyotrophic Lateral Sclerosis in an FUS-Mutated Patient: A Case Report.

Luigi Fiondella, Francesco Cavallieri, Elena Canali, Maria Paola Cabboi, Alessandro Marti, Francesca Sireci, Alena Fiocchi, Gloria Montanari, Sara Montepietra, Franco Valzania

Open access · goldAbstract readCase Reports
In one paragraph

Article in Brain sciences, 2022. 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
0.6field-weighted citation impact, top 32% 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, 5 citations in OpenAlex.

  1. 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

10 authors at 2 institutions in 1 country.

Luigi FiondellaNeurology Unit, Neuromotor and Rehabilitation Department, AUSL-IRCCS of Reggio Emilia, 42123 Reggio Emilia, Italy.ORCID 0000-0001-8170-8948
Francesco CavallieriNeurology Unit, Neuromotor and Rehabilitation Department, AUSL-IRCCS of Reggio Emilia, 42123 Reggio Emilia, Italy.
Elena CanaliNeurology Unit, Neuromotor and Rehabilitation Department, AUSL-IRCCS of Reggio Emilia, 42123 Reggio Emilia, Italy.
Maria Paola CabboiNeurology Unit, Neuromotor and Rehabilitation Department, AUSL-IRCCS of Reggio Emilia, 42123 Reggio Emilia, Italy.
Alessandro MartiNeurology Unit, Neuromotor and Rehabilitation Department, AUSL-IRCCS of Reggio Emilia, 42123 Reggio Emilia, Italy.
Francesca SireciNeurology Unit, Neuromotor and Rehabilitation Department, AUSL-IRCCS of Reggio Emilia, 42123 Reggio Emilia, Italy.
Alena FiocchiPhysical Medicine and Rehabilitation Unit, AUSL-IRCCS of Reggio Emilia, 42123 Reggio Emilia, Italy.
Gloria MontanariPneumology Unit, AUSL-IRCCS of Reggio Emilia, 42123 Reggio Emilia, Italy.
Sara MontepietraNeurology Unit, Neuromotor and Rehabilitation Department, AUSL-IRCCS of Reggio Emilia, 42123 Reggio Emilia, Italy.
Franco ValzaniaNeurology Unit, Neuromotor and Rehabilitation Department, AUSL-IRCCS of Reggio Emilia, 42123 Reggio Emilia, Italy.
Azienda Sanitaria Unità Locale di Reggio Emilia · ITUniversity of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A concomitant presentation of relapsing remitting multiple sclerosis (RRMS) and amyotrophic lateral sclerosis (ALS) is quite rare. However, a review of the literature showed an increased co-occurrence of both diseases, including in genetically determined cases. We report the case of a 49-year-old woman with a history of RRMS who developed a progressive subacute loss of strength in her left arm. The patient’s father died from ALS, and her paternal uncle had Parkinson’s disease. Brain and cervical MRIs were performed, and new demyelinating lesions were excluded. Electromyography (EMG) of the upper limbs showed fibrillations and fasciculations in distal muscles of both arms. In the following months, the patient presented a progressive loss of strength in the proximal and distal muscles of the right arm and hyperreflexia in the lower limbs. EMG and central motor conduction were consistent with ALS. A genetic test was carried out, revealing a mutation in the FUS gene (exon 15; c. 1562 G>A). To our knowledge, the co-occurrence of MS and ALS in patients with FUS mutation is extremely rare. We hypothesize a common pathway for both diseases based on the possibility of a shared oligodendroglial dysfunction due to FUS mutation.

Indexed as

amyotrophic lateral sclerosisclinical neurophysiologyFUSmultiple sclerosisoligodendroglial dysfunction

Identifiers

PMID35624917
PMCPMC9139033
OpenAlexW4224299591

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.