enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Myotonia congenita - Wikipedia

    en.wikipedia.org/wiki/Myotonia_congenita

    Myotonia congenita is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement). It is a genetic disorder.The hallmark of the disease is the failure of initiated contraction to terminate, often referred to as delayed relaxation of the muscles and rigidity. [1]

  3. Limb–girdle muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Limb–girdle_muscular...

    Limb–girdle muscular dystrophy (LGMD) is a genetically heterogeneous group of rare muscular dystrophies that share a set of clinical characteristics. [7] It is characterised by progressive muscle wasting which affects predominantly hip and shoulder muscles. [8]

  4. Myotonia - Wikipedia

    en.wikipedia.org/wiki/Myotonia

    Myotonia is the defining symptom of many channelopathies (diseases of ion channel transport) such as myotonia congenita, paramyotonia congenita and myotonic dystrophy. [3] [4] Brody disease (a disease of ion pump transport) has symptoms similar to myotonia congenita, however, the delayed muscle relaxation is pseudo-myotonia as the EMG is normal ...

  5. Myotonic dystrophy - Wikipedia

    en.wikipedia.org/wiki/Myotonic_dystrophy

    Isolated case reports of myotonia had been published previously, including reports by Frederick Eustace Batten and Hans Curschmann, and type 1 myotonic dystrophy is therefore sometimes known as Curschmann-Batten-Steinert syndrome. [35] The underlying cause of type 1 myotonic dystrophy was determined in 1992. [2]

  6. Myotonic Dystrophy Foundation - Wikipedia

    en.wikipedia.org/wiki/Myotonic_Dystrophy_Foundation

    The Myotonic Dystrophy Foundation (MDF) is a patient organization focused solely on myotonic dystrophy (DM). Based in the Preservation Park of Oakland, California, MDF was founded by families living with myotonic dystrophy. It is an American 501(c)(3) non-profit organization.

  7. Potassium-aggravated myotonia - Wikipedia

    en.wikipedia.org/wiki/Potassium-aggravated_myotonia

    Potassium-aggravated myotonia is a rare genetic disorder that affects skeletal muscle. [2] Beginning in childhood or adolescence, people with this condition experience bouts of sustained muscle tensing ( myotonia ) that prevent muscles from relaxing normally.

  8. Schwartz–Jampel syndrome - Wikipedia

    en.wikipedia.org/wiki/Schwartz–Jampel_syndrome

    Schwartz–Jampel syndrome (SJS, also known as chondrodystrophic myotonia) is a rare genetic disease caused by a mutation in the perlecan gene (HSPG2) [1] which causes osteochondrodysplasia associated with myotonia. [2] Most people with Schwartz–Jampel syndrome have a nearly normal life expectancy. [3]

  9. Fainting goat - Wikipedia

    en.wikipedia.org/wiki/Fainting_goat

    A fainting goat kid in the midst of a myotonic "fainting" spell. The Myotonic Goat or Tennessee fainting goat is an American breed of goat.It is characterised by myotonia congenita, a hereditary condition that may cause it to stiffen or fall over when excited or startled.

  1. Related searches myotonia congenita becker foundation jobs in detroit area free items today

    myotonia congenita wikimyotonia disorder