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Skeletal Muscle Pathology in Autosomal Recessive Cerebellar Ataxias: Insights from Marinesco–Sjögren Syndrome

Academic Article
Publication Date:
2025
abstract:
Cerebellar ataxias are a group of disorders characterized by clumsy movements because of defective muscle control. In affected individuals, muscular impairment might have an impact on activities like walking, balance, hand coordination, speech, and feeding, as well as eye movements. The development of symptoms typically takes place during the span of adolescence, and it has the potential to cause distress for individuals in many areas of their lives, including professional and interpersonal relationships. Although skeletal muscle is understudied in ataxias, its examination may provide hitherto unexplored details in this family of disorders. Observing muscle involvement can assist in diagnosing conditions where genetic tests alone are inconclusive. Furthermore, it helps determine the stage of progression of a pathology that might otherwise be challenging to assess. In this study, we reviewed the main scientific literature reporting on skeletal muscle examination in autosomal recessive cerebellar ataxias (ARCAs), with a focus on the rare Marinesco–Sjögren syndrome. (MSS). Our aim was to highlight the similarities in muscle alterations observed in ARCA patients while also considering data gathered from preclinical models. Analyzing the similarities among these disorders could enhance our understanding of the unidentified mechanisms underlying the phenotypic evolution of some less common conditions.
Iris type:
1.1 Articolo in rivista
Keywords:
cerebellar ataxias; muscle biopsy; preclinical models; skeletal muscle
List of contributors:
Bellia, Fabio; Federici, Luca; Gatta, Valentina; Calabrese, Giuseppe; Sallese, Michele
Authors of the University:
CALABRESE Giuseppe
FEDERICI Luca
GATTA Valentina
SALLESE MICHELE
Handle:
https://ricerca.unich.it/handle/11564/863554
Full Text:
https://ricerca.unich.it//retrieve/handle/11564/863554/557899/ijms-26-06736-v2.pdf
Published in:
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Journal
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URL

https://www.mdpi.com/1422-0067/26/14/6736
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