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Muscular Dystrophy

Breakthrough in Using Stem Cell Therapy to Treat Muscular Dystrophy

Stem cells are unspecialized cells that have not yet differentiated into any specific type. They are unique because they can reproduce themselves infinitely. They can also generate more specialized cell types, such as muscle, nerve or bone cells. They are found in a number of the body’s tissues and organs and occur from the earliest stages of development (embryonic stem cells) to adulthood (adult stem cells). 

At TrueView Biotech we use adult stem cell therapy or umbilical cord stem cells to treat Muscular Dystrophy. 

The ability to create new body tissue means stem cells can use to generate cells to replace diseased and damaged body tissues. These tissues could treat patients whose tissue is diseased or damaged through injury.

Muscular Dystrophy is a group of genetic diseases in which muscle fibers are unusually susceptible to damage. These damaged muscles become progressively weaker. Most people who have muscular dystrophy will eventually need to use a wheelchair.

There are many different kinds of muscular dystrophy. Symptoms of the most common variety begin in childhood, primarily in boys. Other types of muscular dystrophy don't surface until adulthood.

People who have muscular dystrophy may have trouble breathing or swallowing. Their limbs may also draw inward and become fixed in that position — a problem called contracture. Some varieties of the disease can also affect the heart and other organs.

Progressive muscle weakness is the main feature of muscular dystrophy. Each separate form of muscular dystrophy varies a bit in terms of the age at which the signs and symptoms usually begin and the sequence in which different muscle groups are affected.

Duchenne muscular dystrophy

About half of all muscular dystrophy cases are the Duchenne variety, which most commonly occurs in boys. Signs and symptoms typically first surface when the child begins to walk and may include:

. Frequent falls

. Difficulty getting up from a lying or sitting position

. Trouble running and jumping

. Waddling gait

. Large calf muscles

. Learning disabilities

Becker muscular dystrophy 

This variety has signs and symptoms similar to Duchenne muscular dystrophy, but they typically are milder and progress more slowly. Symptom onset is generally in the teens but may not occur until the mid-20s or even later.

Other types of muscular dystrophy:

Certain other types of muscular dystrophy are defined by a specific feature or the location of the body where symptoms first begin. Examples include:

Myotonic. Also known as Steinert's disease, this form of muscular dystrophy also features an inability to relax muscles at will. It most often begins in early adulthood. Muscles of the face are usually the first to be affected.  

Limb-girdle. The hip and shoulder muscles are usually the first affected in this type of muscular dystrophy. In some cases, it becomes difficult to lift the front part of the foot, so frequent tripping may occur. Signs and symptoms may begin from early childhood to adulthood.

Congenital. This category of muscular dystrophy is apparent at birth or becomes evident before age 2. Some forms progress slowly and cause only mild disability, while others progress rapidly and cause severe impairment.

Fascioscapulohumeral (FSHD). One of the most striking signs of this variety of muscular dystrophy is that the shoulder blades might stick out like wings when the person raises his or her arms. Onset usually occurs in teens or young adults.

Oculopharyngeal. The first sign of this type of muscular dystrophy is usually drooping of the eyelids. Weakness of the muscles of the eye, face and throat often results in swallowing difficulties. Signs and symptoms first appear in adulthood, usually in a person's 40s or 50s.

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 Email: info@trueviewbiotech.com

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