What are the symptoms of muscle dystrophy?

There are many different forms of muscle dystrophy, a genetic state characterized by progressive muscle weakness and possible waste of muscles. Recognizing the symptoms of muscle dystrophy can help people identify the condition in the early stages, which can allow them more opportunities for treatment and intervention. Especially in families with a history of disease, it is important to pay attention to the symptoms of early warning and consider genetic advice to discuss the consequences of the family history. However, when the child begins to tod, signs of muscle weakness such as increased fatigue, problems with sitting, walking, throwing and problems. The patient may also experience the symptoms of muscle dystrophy, such as frequent falls, problems with the classroom or terrain changes and abnormalities of walking such as foot walking.

As a musc. In some patients, the symptoms of muscle dystrophy may not occur until adolescence or dThe drowsiness and the form of muscle dystrophy involved is usually mild. Other patients experience the onset of symptoms at a very early childhood or childhood. Over time, the patient may lose the ability to walk and experience a serious compromise of joints caused by contracture (or shortening) in the muscles that surround the joints, leading to a reduced range of movement for the patient.

This condition is most commonly seen in boys, because these are features linked to X. In boys, x-bound features are displayed because they inherit a copy of the defective gene in the X chromosome and the chromosome Y does not have genetic material to balance the defective gene. Women can be Carriers muscle dystrophy, but often do not develop a condition because they need two defective x chromosomes. Some women develop mild symptoms of muscle dystrophy, when they are carriers, depending on what form they carry.

If the symptoms of muscle dystrophy are identified in the childÉkář use the blood test creatine kinase as a timely diagnostic tool. If the test detects abnormalities, the physician may recommend genetic testing to determine which form of muscle dystrophy is involved, using this information to develop treatment recommendations and a long -term patient plan. Medible treatment can radically improve the quality of life and independence for the patient, except for the potential increase in the patient's life.