paramyotonia congenita , PC (Abkürzung)
Eulenburg disease

There has been one study of a large number of patients with paramyotonia congenita.

Some patients do not require treatment to manage the symptoms of paramyotonia congenita.

Some patients also indicate that specific foods are able to induce symptoms of paramyotonia congenita.

The primary symptom of paramyotonia congenita is muscle contracture which develops during exercise or activity.

There is also a disorder called Paramyotonia Congenita.

It occurs in paramyotonia congenita.

He was the first to describe a rare muscular condition known as paramyotonia congenita, which is sometimes referred to as "Eulenburg's disease".

This means people with both hyperkalemic periodic paralysis and paramyotonia congenita can have attacks with fluctuations of potassium up or down.

Myotonia is present in Myotonia congenita, Paramyotonia Congenita and myotonic dystrophy.

Paramyotonia congenita (PC) and potassium aggravated myotonias (PAM)

Mutations in the gene are associated with hypokalemic periodic paralysis, hyperkalemic periodic paralysis, paramyotonia congenita, and potassium-aggravated myotonia.

Paramyotonia congenita (as well as hyperkalemic periodic paralysis and the potassium-aggravated myotonias) is caused by mutations in a sodium channel, SCN4A.

However, myotonia caused by CLCN1 mutations can occasionally be clinically indistinguishable from myotonia caused by sodium channel mutations (SCN4A mutations) resulting in the similar disease 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.

Eulenburg Disease Myotonia Congenita Intermittens Paralysis Periodica Paramyotonica Paramyotonia Congenita of Von Eulenburg Von Eulenburg Paramyotonia Congenita None Paramyotonia congenita is a rare muscular disorder inherited as an autosomal dominant trait.

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.

Eulenburg Disease Myotonia Congenita Intermittens Paralysis Periodica Paramyotonica Paramyotonia Congenita of Von Eulenburg Von Eulenburg Paramyotonia Congenita None Paramyotonia congenita is a rare muscular disorder inherited as an autosomal dominant trait.