Cargando…
Congenital myopathies: clinical phenotypes and new diagnostic tools
Congenital myopathies are a group of genetic muscle disorders characterized clinically by hypotonia and weakness, usually from birth, and a static or slowly progressive clinical course. Historically, congenital myopathies have been classified on the basis of major morphological features seen on musc...
Autores principales: | Cassandrini, Denise, Trovato, Rosanna, Rubegni, Anna, Lenzi, Sara, Fiorillo, Chiara, Baldacci, Jacopo, Minetti, Carlo, Astrea, Guja, Bruno, Claudio, Santorelli, Filippo M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688763/ https://www.ncbi.nlm.nih.gov/pubmed/29141652 http://dx.doi.org/10.1186/s13052-017-0419-z |
Ejemplares similares
-
Myoimaging in the NGS era: the discovery of a novel mutation in MYH7 in a family with distal myopathy and core-like features – a case report
por: Astrea, Guja, et al.
Publicado: (2016) -
P-5
Search for mutations in the RYR1 gene in Italian
patients with congenital myopathy
por: Cassandrini, D., et al.
Publicado: (2011) -
Automatic Recognition of Ragged Red Fibers in Muscle Biopsy from Patients with Mitochondrial Disorders
por: Baldacci, Jacopo, et al.
Publicado: (2022) -
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype–Genotype Correlations: The Example of RYR1-Related Myopathies
por: Dosi, Claudia, et al.
Publicado: (2023) -
Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature
por: Marinella, Gemma, et al.
Publicado: (2023)