Myopathy with extrapyramidal signs

From WikiMD's Medical Encyclopedia

Revision as of 17:44, 7 April 2021 by Deepika vegiraju (talk | contribs) (Created page with "== '''Alternate names''' == Proximal myopathy with extrapyramidal signs == '''Definition''' == Myopathy with extrapyramidal signs is a disorder characterized by early childho...")
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

Alternate names

Proximal myopathy with extrapyramidal signs

Definition

Myopathy with extrapyramidal signs is a disorder characterized by early childhood onset of proximal muscle weakness (muscles closest to the body’s midline) and learning disabilities.

Cause

It is caused by changes (mutations) in the MICU1 gene.

Inheritance

Autosomal recessive inheritance, a 25% chance

This condition is inherited in an autosomal recessive pattern.

Signs and symptoms

  • This condition is characterized by early childhood onset of proximal muscle weakness (muscles closest to the body’s midline) and learning disabilities. The muscle weakness does not progress, but most patients develop progressive atypical involuntary muscle contractions that influence gait, movement, and posture (extrapyramidal signs) that may be disabling.
  • Signs and symptoms are variable and include brief, repetitive, jerky and uncontrolled movements caused by muscle contractions (chorea), tremor, abnormal posturing, and involuntary repetitive movements of the mouth and face.
  • Other symptoms may include uncoordinated movements (ataxia), a very small head (microcephaly), drooping of the eyelids, wasting of the eye nerve (optic atrophy), and axonal peripheral neuropathy.

Clinical presentation

For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed.

30%-79% of people have these symptoms

  • Abnormal basal ganglia MRI signal intensity
  • Central core regions in muscle fibers
  • Centrally nucleated skeletal muscle fibers
  • Chorea
  • Difficulty running
  • Difficulty walking(Difficulty in walking)
  • Dystonia
  • Global developmental delay
  • Increased variability in muscle fiber diameter
  • Orofacial dyskinesia
  • Progressive extrapyramidal movement disorder
  • Progressive extrapyramidal muscular rigidity
  • Proximal muscle weakness(Weakness in muscles of upper arms and upper legs)
  • Resting tremor(Tremor at rest)

5%-29% of people have these symptoms

1%-4% of people have these symptoms

  • Abnormality of extrapyramidal motor function
  • Specific learning disability
  • Tremor

Diagnosis

Treatment

NIH genetic and rare disease info

Myopathy with extrapyramidal signs is a rare disease.


Resources

Message
No content specified



Stub icon
   This article is a Myopathy with extrapyramidal signs stub. You can help WikiMD by expanding it!






<html><link rel="canonical" href="https://wikimd.com/wiki/Myopathy+with+extrapyramidal+signs">‎ <meta name=”viewport” content=”width=device-width, initial-scale=1″> </html>

Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Ad. Transform your health with W8MD Weight Loss, Sleep & MedSpa

W8MD's happy loser(weight)

Tired of being overweight?

Special offer:

Budget GLP-1 weight loss medications

  • Semaglutide starting from $29.99/week and up with insurance for visit of $59.99 and up per week self pay.
  • Tirzepatide starting from $45.00/week and up (dose dependent) or $69.99/week and up self pay

✔ Same-week appointments, evenings & weekends

Learn more:

Advertise on WikiMD


WikiMD Medical Encyclopedia

Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.