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A Novel Method for Detecting Duchenne Muscular Dystrophy in Blood Serum of mdx Mice

Authors :
Nicole M. Ralbovsky
Paromita Dey
Andrew Galfano
Bijan K. Dey
Igor K. Lednev
Source :
Genes. 13:1342
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy, typically affecting males in infancy. The disease causes progressive weakness and atrophy of skeletal muscles, with approximately 20,000 new cases diagnosed yearly. Currently, methods for diagnosing DMD are invasive, laborious, and unable to make accurate early detections. While there is no cure for DMD, there are limited treatments available for managing symptoms. As such, there is a crucial unmet need to develop a simple and non-invasive method for accurately detecting DMD as early as possible. Raman spectroscopy with chemometric analysis is shown to have the potential to fill this diagnostic need.

Subjects

Subjects :
Genetics
Genetics (clinical)

Details

ISSN :
20734425
Volume :
13
Database :
OpenAIRE
Journal :
Genes
Accession number :
edsair.doi...........9f9c0c8103c6975e9283dd39b00cdb07
Full Text :
https://doi.org/10.3390/genes13081342