Congenital myopathy refers to a type of degenerative muscular disorder caused by genetic abnormalities the infant inherits from his or her parents. Although congenital myopathies can be extremely debilitating, advancements in technology have allowed medical professionals to recommend suitable treatments that typically increase these patients' quality of life.
While congenital myopathies are present in patients from birth, they may not be detected until the child starts walking and physically developing. In general, however, doctors diagnose congenital myopathy in patients before they hit their later teen years.
In this section, we will take a closer look at the symptoms of and treatments for various types of congenital myopathies. Our articles will highlight some of the newest treatment options, along with the pros and cons associated with each.
The exact way in which congenital myopathy will affect a patient will depend on the precise condition he has. The following lists the five most common types of congenital myopathy, including the unique symptoms of each:
As with other types of myopathy, the symptoms of congenital myopathies will vary depending on:
However, those suffering from a congenital myopathy will likely experience any combination of the following symptoms:
If you have a family history of congenital myopathy, be sure you understand and are aware of congenital myopathy symptoms.
Because no cure currently exists for any type of myopathy, treatments for congenital myopathies revolve around decreasing the condition's symptoms and improving the patient's quality of life. Any combination of the following is suitable treatment for congenital myopathy patients:
If you currently suffer from congenital myopathy, talk to your doctor about the most appropriate combination of congenital myopathy treatments for you.
Mayo Clinic (n.d.) Congenital Myopathies. Retrieved January 3, 2008, from the Mayo Clinic Web site: http://www.mayoclinic.org/congenital-myopathies/.
Merck (updated November 2005). Congenital Myopathies. Retrieved January 3, 2008, from the Merck Web site: http://www.merck.com/mmpe/sec19/ch295/ch295c.html.
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