Searching for Myotonia Congenita Support information? Find all needed info by using official links provided below.
https://ghr.nlm.nih.gov/condition/myotonia-congenita
Oct 29, 2019 · Myotonia congenita is a disorder that affects muscles used for movement (skeletal muscles).Beginning in childhood, people with this condition experience bouts of sustained muscle tensing (myotonia) that prevent muscles from relaxing normally.
https://rarediseases.info.nih.gov/diseases/12301/myotonia-congenita
Mar 22, 2017 · Myotonia congenita is a genetic disease characterized by the inability of the skeletal muscles to quickly relax after voluntary movements. Symptoms typically begin in childhood and vary from person to person. They may include muscle stiffness, muscle weakness, and attacks of weakness brought on by movement after rest. There are two forms of myotonia …
https://www.mda.org/disease/myotonia-congenita
What is myotonia congenita? Myotonia congenita is an inherited myopathy, a disease that causes problems with the tone and contraction of skeletal muscles. It doesn’t cause muscle atrophy (shrinkage); instead, it sometimes can cause muscle enlargement and increased muscle strength. There are two types of myotonia congenita: Becker-type myotonia is the most common form, …
https://www.ninds.nih.gov/disorders/all-disorders/myotonia-congenita-information-page
Myotonia congenita is an inherited neuromuscular disorder characterized by the inability of muscles to quickly relax after a voluntary contraction. The condition is present from early childhood, but symptoms can be mild.
https://rarediseases.org/rare-diseases/myotonia-congenita/
Myotonia congenita is a rare genetic disorder in which an abnormality of voluntary (skeletal) muscle fiber membranes causes an unusually exaggerated response to stimulation (hyperexcitability). ... Special services that may be beneficial include special social support, physical therapy, and/or other medical, social, and/or vocational services.
https://www.myotonic.org/find-support
For those who do not live near one of our existing support groups, our online support community is available at any time. The Myotonic Caregivers Support Group is a confidential, virtual support group that meets monthly via webinars. We also offer Facebook Live Chats on the first and third Tuesday of every month.
https://www.ncbi.nlm.nih.gov/books/NBK1355/
Aug 03, 2005 · Myotonia congenita is characterized by muscle stiffness present from childhood; all striated muscle groups including the extrinsic eye muscles, facial muscles, and tongue may be involved. Stiffness is relieved by repeated contractions of the muscle (the “warm-up” phenomenon). Muscles are usually hypertrophic. The autosomal recessive form of myotonia …
https://www.mountsinai.org/health-library/diseases-conditions/myotonia-congenita
Myotonia congenita is caused by a genetic change (mutation). It is passed down from either one or both parents to their children (inherited). Myotonia congenita is caused by a problem in the part of the muscle cells that are needed for muscles to relax. Abnormal repeated electrical signals occur in the muscles, causing a stiffness called myotonia.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562961/
Aug 15, 2017 · Myotonia congenita (MC) is a nondystrophic myotonic disorder (NDM) caused by CLCN1 chloride channel mutations resulting in a reduction of chloride conductance. MC results in impairment due to symptoms of muscle stiffness without altering the life span, and among the NDMs, MC has the greatest detrimental effect on patients' perceived quality of life. 1Cited by: 9
https://ghr.nlm.nih.gov/condition/myotonia-congenita
Oct 29, 2019 · Myotonia congenita is a disorder that affects muscles used for movement (skeletal muscles).Beginning in childhood, people with this condition experience bouts of sustained muscle tensing (myotonia) that prevent muscles from relaxing normally.
https://www.diseaseinfosearch.org/disease/5074/support
Are you looking for disease information or support? Simply type in the name of a disease or condition and Disease InfoSearch will locate quality information from a database of more than 13,000 diseases and thousands of support groups and foundations.
https://www.ninds.nih.gov/disorders/all-disorders/myotonia-congenita-information-page
Myotonia congenita is an inherited neuromuscular disorder characterized by the inability of muscles to quickly relax after a voluntary contraction. The condition is present from early childhood, but symptoms can be mild.
https://www.verywellhealth.com/myotonia-congenita-overview-4178016
Myotonia congenita, also called congenita myotonia, is a rare, genetic disease that begins during childhood and causes muscle stiffness and cramping.If you or your child have myotonia congenita, you should know that while the condition causes bothersome symptoms, it can be managed with therapy and medication once it is diagnosed.
https://www.mountsinai.org/health-library/diseases-conditions/myotonia-congenita
Myotonia congenita is caused by a genetic change (mutation). It is passed down from either one or both parents to their children (inherited). Myotonia congenita is caused by a problem in the part of the muscle cells that are needed for muscles to relax. Abnormal repeated electrical signals occur in the muscles, causing a stiffness called myotonia.
https://rarediseases.info.nih.gov/diseases/12301/myotonia-congenita
Mar 22, 2017 · Myotonia congenita is a genetic disease characterized by the inability of the skeletal muscles to quickly relax after voluntary movements. Symptoms typically begin in childhood and vary from person to person. They may include muscle stiffness, muscle weakness, and attacks of weakness brought on by movement after rest. There are two forms of myotonia congenita…
https://www.mda.org/disease/myotonia-congenita
What is myotonia congenita? Myotonia congenita is an inherited myopathy, a disease that causes problems with the tone and contraction of skeletal muscles. It doesn’t cause muscle atrophy (shrinkage); instead, it sometimes can cause muscle enlargement and increased muscle strength. There are two types of myotonia congenita: Becker-type myotonia is the most …
https://rarediseases.org/rare-diseases/myotonia-congenita/
Myotonia congenita is a rare genetic disorder in which an abnormality of voluntary (skeletal) muscle fiber membranes causes an unusually exaggerated response to stimulation (hyperexcitability). ... Special services that may be beneficial include special social support, physical therapy, and/or other medical, social, and/or vocational services.
https://www.myotonic.org/find-support
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