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
Myotonic dystrophy does not have attributed behavior problems per se. However, Childhood and adolescent forms of the disease can exhibit cognitive difficulties which can present in a number of different ways such as attention deficit type disorders which could be mislabeled as behavior problems. Your best source of information on Myotonic Dystrophy on the web is the Myotonic Dystrophy Foundation.
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.
Yes, there are prenatal tests available for myotonic dystrophy. These tests can include genetic testing of the fetus through procedures like chorionic villus sampling (CVS) or amniocentesis, which analyze fetal DNA for the presence of the gene mutations associated with myotonic dystrophy. Additionally, if there is a known family history, preimplantation genetic diagnosis (PGD) can be used in conjunction with in vitro fertilization (IVF) to select embryos that do not carry the mutation. Consulting with a genetic counselor can provide more personalized information and guidance.
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