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INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT International Peer Reviewed & Refereed Journals, Open Access Journal ISSN Approved Journal No: 2456-4184 | Impact factor: 8.76 | ESTD Year: 2016 Scholarly open access journals, Peer-reviewed, and Refereed Journals, Impact factor 8.76 (Calculate by google scholar and Semantic Scholar | AI-Powered Research Tool) , Multidisciplinary, Monthly, Indexing in all major database & Metadata, Citation Generator, Digital Object Identifier(DOI) |
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| Paper Title: | A REVIEW ON DUCHENNE MUSCULAR DYSTROPHY |
| Authors Name: | Landge Avirali Balasaheb , Vhalgade Nikita R. , Suryawanshi Parinita B. , Suryawanshi Rutuja S. , Sonar Ankita D. |
| Download E-Certificate: | Download |
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IJNRD_185118
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| Published Paper Id: | IJNRD2212214 |
| Published In: | Volume 7 Issue 12, December-2022 |
| DOI: | |
| Abstract: | Duchenne Muscular Dystrophy is an inherited neuromuscular disorder caused by gene mutation i.e. dystrophin protein which is responsible for the structure and functions of the muscles. It is characterized by specific abnormalities in the muscle biopsy of the patients in which the muscles in the body weakens day by day and loosens its functions. DMD mostly occurs in the boys approximately 1/3500 male births worldwide, while females are normally carriers. The disease progression is fast as compare to other types of muscular dystrophy. Typically, symptoms start in early childhood. Children with DMD struggle to walk, stand up, and climb stairs. Many eventually require wheelchairs in order to move about. They may also experience heart and lung issues. The outlook for those who have DMD is brighter than it has ever been, despite the lack of a cure. Children with the condition used to typically not live past their adolescent years. They frequently live into their 30s and 40s today and live well into their 20s. There are treatments like gene therapy, physiotherapy, drug therapy that can reduce symptoms, and scientists are also exploring for new ones. |
| Keywords: | DMD; Muscular dystrophy, Duchenne; Muscular dystrophy, progressive, Duchenne type; Duchenne Muscular Dystrophy; Dystrophinopathy; Dystrophin, heredity, chromosome, physiotherapy, corticosteroids, etc. |
| Cite Article: | "A REVIEW ON DUCHENNE MUSCULAR DYSTROPHY", International Journal of Novel Research and Development (www.ijnrd.org), ISSN:2456-4184, Vol.7, Issue 12, page no.c96-c107, December-2022, Available :http://www.ijnrd.org/papers/IJNRD2212214.pdf |
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| ISSN: |
2456-4184 | IMPACT FACTOR: 8.76 Calculated By Google Scholar| ESTD YEAR: 2016 An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.76 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator |
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Published Paper ID:IJNRD2212214 Registration ID: 185118 Published In: Volume 7 Issue 12, December-2022 DOI (Digital Object Identifier): Page No: c96-c107 Country: Nashik, Maharashtra, India Research Area: Pharmacy Publisher : IJ Publication Published Paper URL : https://www.ijnrd.org/viewpaperforall?paper=IJNRD2212214 Published Paper PDF: https://www.ijnrd.org/papers/IJNRD2212214 |
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ISSN: 2456-4184
Impact Factor: 8.76 and ISSN APPROVED
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