Understanding Duchenne Muscular Dystrophy (DMD)
Duchenne Muscular Dystrophy is a severe genetic disorder marked by progressive muscle weakness. It's primarily seen in boys and begins in early childhood. This section aims to provide a detailed understanding of DMD, covering its symptoms, such as early muscle weakness, difficulties in walking, and enlargement of calf muscles. We also explore the diagnostic methods including genetic testing and muscle biopsies, and the challenges faced by those living with DMD, emphasizing the importance of comprehensive care and support.
Other Related Muscular Conditions
In addition to DMD, there are several other muscular dystrophies and atrophies, each with unique characteristics. This part of the section provides an overview of conditions like Becker Muscular Dystrophy, Limb-Girdle Muscular Dystrophy, and Spinal Muscular Atrophy, discussing their symptoms, diagnosis, and management. Understanding these conditions is crucial for providing appropriate care and support to those affected.