Evidence map›Paper›PMID 34925671›Full record

ArticleRadiology case reports2022

Mucopolysaccharidosis type IV: report of 5 cases of Morquio Syndrome.

Jorge Alejandro Cadena Arteaga, Fabricio Andres Lasso Andrade, Denny Marcela Achicanoy Puchana, Diana Fernanda Achicanoy Puchana, Gina Natalia Caicedo Morillo, Paola Andrea Medina Bravo, William Fernando Juez Neira, Cristian Ricardo Vanegas Bastidas, Diana Carolina Montoya Ríos, Karen Julieth Vasquez Correa and 2 more

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PubMed Full text at PMC Publisher
In one paragraph

Article in Radiology case reports, 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
0.1field-weighted citation impact, top 51% 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, 4 citations in OpenAlex.

  1. 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

12 authors at 9 institutions in 2 countries.

Jorge Alejandro Cadena ArteagaEspecialista en Radiología. Universidad del Valle. Cali, Valle del Cauca- Colombia.
Fabricio Andres Lasso AndradeUniversidad del Cauca. Especialista Epidemiología, Universidad Autónoma de Bucaramanga. Residente Anestesiología y Reanimación, Universidad Nacional de Colombia.
Denny Marcela Achicanoy PuchanaUniversidad de Nariño. Residente de Imagenología diagnóstica y terapéutica, Universidad Nacional Autónoma de México.
Diana Fernanda Achicanoy PuchanaUniversidad de Nariño. Residente de Imagenología diagnóstica y terapéutica, Universidad Nacional Autónoma de México.
Gina Natalia Caicedo MorilloUniversidad de Antioquia. MSP. Gerencia de la Seguridad y Salud en el Trabajo, Universidad Iberoamericana.
Paola Andrea Medina BravoUniversidad El Bosque.
William Fernando Juez NeiraUniversidad del Valle.
Cristian Ricardo Vanegas BastidasUniversidad Tecnológica de Pereira.
Diana Carolina Montoya RíosUniversidad de Manizales.
Karen Julieth Vasquez CorreaUniversidad de Antioquia.
Laura Catalina Suárez CuéllarUniversidad Cooperativa de Colombia.
Lady Johana Osorio SeguraUniversidad del Valle.
Universidad del Valle · COUniversidad Nacional Autónoma de México · MXIbero American University · MXTechnological University of Pereira · COUniversidad Autónoma de Bucaramanga · COUniversidad Cooperativa de Colombia · COUniversidad de Antioquia · COUniversidad de Manizales · COUniversidad El Bosque · CO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucopolysaccharidosis type IV or Morquio Syndrome, is a lysosomal deposit disease, of autosomal recessive inheritance with a similar incidence in men and women. The clinical picture is of variable expressiveness, its phenotype is characterized by skeletal dysplasia that includes neck and short trunk, short stature, keel thorax, kyphosis, scoliosis, genus valgus, flat foot, coxa valga, gait disorders, instability of the cervical spine and wedge or ovoid vertebrae. The treatment is symptomatic, with enzyme replacement. We present a series of 5 cases, the product of 2 couples, with a confirmed diagnosis of Mucopolysaccharidosis type IV, and different clinical presentation.

Indexed as

GlycosaminoglycansMorquio syndromeMucopolysaccharidosisShort stature

Identifiers

PMID34925671
PMCPMC8649122
OpenAlexW4200037830

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.