(vietnamnet.vn) In world medical literature, there is no "deltoid muscle atrophy", there is only the symptom of delta muscle atrophy and this symptom is seen in many different diseases.

Children with Duchenne muscular dystrophy are genetically characterized by progressive muscle atrophy, even leading to paralysis of the respiratory muscles, causing respiratory failure and death. In addition to the use of internal medicine, rehabilitation is a method to help slow the progression of muscle atrophy and limit the risk of death in children.

Childhood muscular dystrophy is a genetic disease associated with a number of gene mutations. Diseases with a genetic factor play a decisive role, the age of onset is usually quite young, mostly occurring in school-age children and some cases occurring in newborns.

Muscle degeneration and muscle atrophy can cause many abnormalities that affect the health and quality of life of the patient. Therefore, you need to know the early signs of muscle degeneration and muscle atrophy to have early measures to change your lifestyle and intervene in treatment when necessary.

Muscular dystrophy syndromes comprise a group of disorders that cause progressive muscle weakness and eventually muscle atrophy. People with muscular dystrophy have abnormal genes that prevent the production of proteins needed for healthy muscles. There are several types of muscular dystrophy syndromes, with the most common type of progressive muscular dystrophy showing symptoms in childhood and more common in boys. The other types of muscular dystrophy do not appear until adulthood.

Muscular dystrophy is a genetic disease. Although it is not common, the possibility of passing it on to the next generation is quite high. How to treat muscular dystrophy is still a question for the scientific community. However, some current medical achievements are still being applied to diagnose and treat muscular dystrophy.

Metachromatic leukodystrophy is a genetic metabolic disorder. This is a dangerous muscular dystrophy because if not treated promptly, it will cause paralysis, cognitive impairment and even death.