Evidence map›Paper›PMID 35866733›Full record

ArticleBiomedica : revista del Instituto Nacional de Salud2022

Clinical-functional characterization of patients with spinal muscular atrophy in Central-Western Colombia

Natalia Cardona, Sandra Jhoana Ocampo, Jorge Mario Estrada, María Isabel Mojica, Gloria Liliana Porras

Open access · diamondAbstract read
In one paragraph

Article in Biomedica : revista del Instituto Nacional de Salud, 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
0.9field-weighted citation impact, top 26% 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, 6 citations in OpenAlex.

  1. Journal of clinical medicine · 2024
    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

5 authors at 4 institutions in 3 countries.

Natalia CardonaCentro de Enfermedades Huérfanas - ComSentido, Salud Comfamiliar, Comfamiliar Risaralda, Pereira, Colombia; Grupo de Investigación Salud Comfamiliar, Comfamiliar Risaralda, Pereira, Colombia. ncardonar@comfamiliar.com.
Sandra Jhoana OcampoMaestría en Genética Humana, Universidad Nacional de Colombia, Bogotá, D.C., Colombia. socampoma@unal.edu.co.
Jorge Mario EstradaGrupo de Investigación Salud Comfamiliar, Comfamiliar Risaralda, Pereira, Colombia. jestradaa@comfamiliar.com.
María Isabel MojicaGrupo de Investigación Salud Comfamiliar, Comfamiliar Risaralda, Pereira, Colombia. mimojica624@gmail.com.
Gloria Liliana PorrasCentro de Enfermedades Huérfanas - ComSentido, Salud Comfamiliar, Comfamiliar Risaralda, Pereira, Colombia; Grupo de Investigación Salud Comfamiliar, Comfamiliar Risaralda, Pereira, Colombia. gporras@comfamiliar.com.
Centre National de la Recherche Appliquée au Developpement Rural · MGHospital Comarcal de Inca · ESTechnological University of Pereira · COUniversidad Nacional de Colombia · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Spinal muscular atrophy is a rare genetic neurodegenerative disorder affecting the motor neurons of the anterior horn of the spinal cord, which results in muscle atrophy and weakness. In Colombia, few studies have been published on the pathology and none with functional analysis. Objective: To characterize clinically and functionally some cases of spinal muscular atrophy patients from Central-Western Colombia. Materials and methods: We conducted a cross-sectional descriptive study between 2007 and 2020 with patients clinically and molecularly diagnosed with spinal muscular atrophy who attended a care center. For the functional assessment we used the Hammersmith and Chop-Intend scales and the data were systematized with the Epi-Info, version 7.0 software. Results: We analyzed 14 patients (42.8 % men). The most prevalent spinal muscular atrophy was type II with 71.4 %. We found phenotypic variability in terms of functionality in some patients with type II spinal muscular atrophy, 37.5 % of whom reached gait. Survival was estimated at 28.6 years. Conclusions: The findings in the group of patients analyzed revealed that the scores of the revised and expanded Hammersmith scales correlated with the severity of SMA.

Indexed as

Muscular Atrophy, SpinalColombiaCross-Sectional StudiesFemaleHumansMaleRetrospective StudiesMuscular atrophyphysical therapy specialtyrare diseasesspinal

Identifiers

PMID35866733
PMCPMC9410705
OpenAlexW3216025325

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.