Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 

Nemaline myopathy 2

Nemaline myopathy 2: Introduction

Nemaline myopathy 2: A very rare inherited muscle disorder and is characterized by muscle weakness caused by the presence of nemaline rods in the muscle tissue which affects its function. There are at least 7 different subtypes of nemaline myopathy, each with a different genetic defect. The severity of the symptoms may vary greatly even among patients within a particular subtype of the disorder. Type 2 is caused by a defect on the nebulin gene on chromosome 2q22. More detailed information about the symptoms, causes, and treatments of Nemaline myopathy 2 is available below.

Symptoms of Nemaline myopathy 2

Wrongly Diagnosed with Nemaline myopathy 2?

Nemaline myopathy 2: Related Patient Stories

Nemaline myopathy 2: Complications

Review possible medical complications related to Nemaline myopathy 2:

Causes of Nemaline myopathy 2

Read more about causes of Nemaline myopathy 2.

Less Common Symptoms of Nemaline myopathy 2

Nemaline myopathy 2: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Nemaline myopathy 2: Animations

Nemaline myopathy 2: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Nemaline myopathy 2, or answer someone else's question, on our message boards:

 

By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise