Cargando…
Muscle Weakness: A Misleading Presentation in Children With Distinctive Syndromic Entities (Clinical Case Reports)
Marked ligamentous hyperlaxity and muscle weakness/wasting associated with awkward gait are the main deficits confused with the diagnosis of myopathy. Seven children (6 boys and 1 girl with an average age of 8 years) were referred to our department because of diverse forms of skeletal abnormalities....
Autores principales: | Al Kaissi, Ali, Ryabykh, Sergey, Ochirova, Polina, Kenis, Vladimir, Hofstätter, Jochen G., Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5298546/ https://www.ncbi.nlm.nih.gov/pubmed/28210640 http://dx.doi.org/10.1177/2324709616689583 |
Ejemplares similares
-
Spine malformation complex in 3 diverse syndromic entities: Case reports
por: Kaissi, Ali Al, et al.
Publicado: (2016) -
The Managment of cervical spine abnormalities in children with spondyloepiphyseal dysplasia congenita: Observational study
por: Al Kaissi, Ali, et al.
Publicado: (2019) -
Torticollis in Connection with Spine Phenotype
por: Al Kaissi, Ali, et al.
Publicado: (2022) -
Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan
por: Al Kaissi, Ali, et al.
Publicado: (2019) -
Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review Article
por: Kaissi, Ali Al, et al.
Publicado: (2020)