Myotonic Dystrophy: A Genetic Disorder Causing Progressive Muscle Wasting

This poster provides an overview of Myotonic Dystrophy (DM), a genetic disorder characterized by progressive muscle wasting and weakness. It highlights the differences between DM1 and DM2, the genetic mechanisms involved, clinical features, and the pathogenesis of the disease. The aim is to raise awareness and understanding of this inherited condition among medical and scientific communities.

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-05-18
DOI
https://doi.org/10.5281/zenodo.15460124
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.00
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article

Myotonic Dystrophy: A Genetic Disorder Causing Progressive Muscle Wasting

Zenodo (CERN European Organization for Nuclear Research)
Genetic Neurodegenerative Diseases
article

Myotonic Dystrophy: A Genetic Disorder Causing Progressive Muscle Wasting

article en

Abstract

This poster provides an overview of Myotonic Dystrophy (DM), a genetic disorder characterized by progressive muscle wasting and weakness. It highlights the differences between DM1 and DM2, the genetic mechanisms involved, clinical features, and the pathogenesis of the disease. The aim is to raise awareness and understanding of this inherited condition among medical and scientific communities.

Zenodo (CERN European Organization for Nuclear Research)
Good health and well-being
Openalex Percentile: Top 48%
Genetic Neurodegenerative Diseases
DOIOpen Access PDFOpenAlex
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Myotonic Dystrophy: A Genetic Disorder Causing Progressive Muscle Wasting · Zenodo (CERN European Organization for Nuclear Research) (2025) | TGRS Research Map | TGRS