Do you mean an EKG or EMG? An EKG monitors the heart and an EMG is used to detect abnormal electrical activity within the muscle. I'm not a doctor and I'm not entirely certain that either of the two would not be able to pick up the effects of neuropathy however any sings of it from these tests would probably be implicit rather than explicit as, if it did show up, I'd imagine it be in the form of signal distortion. There is another test which tests the speed the impulses travel through the nerves which I imagine is used more frequently to Dx neuropathy.
Myotonic dystrophy is diagnosed clinically in individuals that have a specific type of muscle weakness. This is confirmed with molecular genetics testing, where the DMPK is analyzed
Yes, Myotonic dystrophy can be associated with cognitive and psychiatric manifestations, such as cognitive impairments, inattention, irritability, and depression. These behavioral problems can vary in severity and may require treatment by healthcare professionals.
Symptoms in the congenital form of myotonic dystrophy are evident at birth. Affected infants show muscle weakness, respiratory defects, and eventually, mental retardation
Myotonic dystrophy cannot be cured, and no treatment can delay its progression. As of the early 2000s there is no standardized treatment for these disorders because the precise reasons for muscle weakness are not yet fully understood.
People who have myotonic dystrophy have progressive muscle wasting and weakness beginning in their 20's or 30's. The muscle wasting and weakness develop in their lower legs, hands, neck and face.
limitations resulting from myotonic dystrophy can be significant, involving muscle weakness and difficulty lifting items and performing certain routine daily tasks. There are many cases in which affected persons experience mental delays
Yes, myotonic dystrophy affects people in multiple ways and can often affect other systems of the body before the skeletal muscles therefore an EMG is no longer a reliable diagnostic tool.
affects heart muscle, causing arrhythmias and heart block, and the muscles of the digestive system, leading to motility disorders and constipation. Other body systems are affected as well: Myotonic dystrophy may cause cataracts
stated to be 1 in 8000 in the USA, a few places have a higher incidence rate
Myotonic dystrophy is considered a rare disorder because its prevalence is estimated to be around 1 in 8,000 individuals. It is caused by a genetic mutation and can affect multiple body systems, leading to muscle weakness, myotonia, and other symptoms. Due to its rarity, it may be underdiagnosed or misdiagnosed in some cases.
facial weakness and a slack jaw, drooping eyelids (ptosis ), and muscle wasting in the forearms and calves. A person with this dystrophy has difficulty relaxing his grasp, especially if the object is cold
There is a chance that your children could inherit myotonic dystrophy if your spouse has the condition. Myotonic dystrophy is an inherited genetic disorder that can be passed on to the next generation. However, the likelihood of passing on the condition and the severity of symptoms can vary among children. Consulting a genetic counselor can provide more personalized information about the risks.