In diagnosing any form of muscular dystrophy, a doctor usually begins by taking a patient and family history and performing a physical examination. Much can be learned from these, including the pattern of weakness. The history and physical go a long way toward making the diagnosis, even before any laboratory tests are done.
The doctor also wants to determine whether the patient’s weakness results from a problem in the muscles themselves (as is the case in muscular dystrophy), or in the muscle-controlling nerves, called motor neurons, that control them.
Early in the diagnostic process, doctors often order a special blood test called a CK level . CK stands for creatine kinase, an enzyme that leaks out of damaged muscle. When elevated CK levels are found in a blood sample, it usually means muscle is being destroyed by some abnormal process, such as a muscular dystrophy or inflammation. Therefore, a high CK level suggests that the muscles themselves are the likely cause of the weakness, but it doesn’t tell exactly what the muscle disorder might be.
Sometimes, special testing called electromyography  is done. In this kind of test, the electrical activity of the muscles is measured and nerves stimulated to see where the problem lies. Electromyography is uncomfortable but not usually very painful.
Today, DNA testing is available for several forms of LGMD and is rapidly expanding. If a particular type of LGMD is suspected, DNA testing (from a blood sample) may be undertaken relatively early in the diagnostic process, often before the doctor considers a more invasive procedure.
In some cases it is necessary for a doctor to order a muscle biopsy , the surgical removal of a small sample of muscle from the patient. By examining this sample, doctors can tell a great deal about what’s actually happening inside the muscles. Using a variety of techniques, muscular dystrophies can be distinguished from inflammatory and other disorders. Specific testing of the biopsy also may distinguish among different forms of muscular dystrophy.
Tests on the biopsy sample also can provide information about which muscle proteins are present in the muscle cells, and whether they’re present in the normal amounts and in the right locations. This can reveal what’s wrong with the cells’ proteins and point toward the genes that may be responsible for the problem. The correlation between missing proteins on the muscle biopsy and genetic flaws isn’t perfect, however.
Genetic testing  is commercially available that can determine the exact type of several, but not all, forms of LGMD. If there are clues as to what gene is involved (from previously tested family members, biopsy findings or symptoms clearly associated with one or two types of LGMD), it may be practical to do DNA testing to pinpoint the gene defect. However, if there are no such clues, testing can get very expensive.
Understanding your inheritance pattern  may, however, be important for family planning. Your family history can help determine the inheritance pattern of your disorder.
No matter the exact genetic cause, treatment  is essentially the same for all forms of LGMD — physical and occupational therapy, assistive devices, and monitoring for heart and breathing complications.