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genetic or congenital, muscles, neurology
frequency
rare (U.S.)
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likelyhood by duration of symptoms
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Definition for paramyotonia congenita

Paramyotonia Congenita (PC), also known as Paramyotonia congenita of von Eulenburg or Eulenburg disease, is a rare congenital autosomal dominant neuromuscular disorder characterized by “paradoxical" myotonia. more


some common symptoms
continuous muscle contractions with activity
difficulty relaxing muscles
inability to perform skilled movements
muscle rigidity


some related diagnoses
1 - 5 of 5 diagnoses
periodic paralyses
potassium-aggravated myotonia
myotonic dystrophy
Andersen-Tawil Syndrome
congenital myopathies
  more

do i have 'paramyotonia congenita'?
In addition the following diagnostic tests might be need to help verify the diagnosis:



therapeutic procedures for 'paramyotonia congenita'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for paramyotonia congenita:
therapeutic procedure search results for 'paramyotonia congenita'
1 - 1 of 1 therapeutic procedures
rankings are computer generated. please consult your health care provider.
avoid myotonia triggering factors





web search results for paramyotonia congenita
Results 1 - 50 - paramyotonia congenita
en.wikipedia.org - summary
ghr.nlm.nih.gov - summary
www.ghr.nlm.nih.gov - summary
www.ncbi.nlm.nih.gov - summary
ghr.nlm.nih.gov - summary
www.ncbi.nlm.nih.gov - summary







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