Muscular dystrophy disorders' prevalence in southern Libya: early observations and challenges as first new experience
Article Sidebar
Main Article Content
Abstract
A series of hereditary illnesses known as muscular dystrophy result in progressive muscle weakening and wasting. Muscular dystrophy can take many various forms, and the incidence rates vary depending on the type and the demographic being researched. The study's objective was to determine the prevalence of muscular dystrophy disorders in Libya's southern area, This study also aims to explain the difficulties and challenges faced by the Scientific Committee and its branches in other southern regions as a first experience with muscular dystrophy patients in terms of sorting and diagnosing these cases. 85 patients had highly suspected hereditary muscular dystrophy, 78 of the 85 patients had positive genetic results.
Downloads
Article Details
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
In a brief statement, the rights relate to the publication and distribution of research published in the journal of the Sebha University, where authors who have published their articles in the Sebha University journal can use or distribute their articles. They reserve all their rights to the published works, such as (but not limited to) the following rights:
- Copyright and other property rights related to the article, such as patent rights.
- Research published in the journal of the University of Sebha and used in its future works, including lectures and books, the right to reproduce articles for their own purposes, and the right to self-archive their articles.
- The right to enter a separate article, or for a non-exclusive distribution of their article with an acknowledgment of its initial publication in the journal of Sebha University.
- Privacy Statement The names and e-mail addresses entered on the Sebha University Journal site will be used for the aforementioned purposes only and for which they were used.
