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Paramyotonia congenita is usually mild enough not to require any treatment at all. If muscle stiffness is truly problematic, quinine or anticonvulsant medications (such as phenytoin) may improve functioning.

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14y ago

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What doctors treat Paramyotonia congenita?

Paramyotonia congenita is diagnosed and treated by neurologists.


What causes Paramyotonia congenita?

Paramyotonia congenita is believed to be caused by a defect in the chloride channels of the muscles.


What is Paramyotonia congenita?

Paramyotonia congenita is an inherited condition that causes stiffness and enlargement of muscles, particularly leg muscles.


What type of hereditary condition is Paramyotonia congenita?

Paramyotonia congenita is passed on in families as an autosomal dominant trait. This means that males and females are affected equally


What are the symptoms of Paramyotonia congenita?

Symptoms of paramyotonia congenita include muscle stiffness and weakness that worsens with exercise or cold temperatures. Individuals may experience muscle pain, cramps, and difficulty relaxing muscles after contraction. These symptoms are typically seen in the face, neck, and hands.


What is the average age of onset for Paramyotonia congenita?

The average age of onset for Paramyotonia congenita is typically around 10 years old, but symptoms can present at any age from infancy to adulthood. It is an inherited condition that affects skeletal muscle function and can cause muscle stiffness and weakness exacerbated by cold temperatures or exercise.


What are the odds of passing Paramyotonia congenita to a child?

if one parent has the trait, the offspring have a 75% chance of also having the condition


What is the prognosis for Paramyotonia congenita?

Although annoying, it does not cause significant disability, and the patient usually learns to make lifestyle adjustments that prevent exacerbations (for example, dressing warmly and avoiding exposure to cold).


Is there any medication for myotonia congenita?

mexilitine, quinine,


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