Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 11 for Myoclonic epilepsy myopathy sensory ataxia
  1. Myoclonic epilepsy myopathy sensory ataxia, commonly called MEMSA, is part of a group of conditions called the POLG-related disorders. The conditions in this group ...
  2. Cerebellar Disorders (National Library of Medicine)  
    When you play the piano or hit a tennis ball you are activating the cerebellum. The cerebellum is the area of the brain that controls coordination and balance. ...
  3. Movement Disorders (National Library of Medicine)  
    Movement disorders are neurologic conditions that cause problems with movement, such as: Increased movement that can be voluntary (intentional) or involuntary ( ...
  4. Seizures (National Library of Medicine)  
    Seizures are symptoms of a brain problem. They happen because of sudden, abnormal electrical activity in the brain. When people think of seizures, they often ...
  5. ... POLG gene cause another POLG-related disorder called myoclonic epilepsy myopathy sensory ataxia (MEMSA), which is characterized by recurrent seizures (epilepsy), ...
  6. ... in a few people with variant forms of myoclonic epilepsy with ragged-red fibers ... hearing loss, seizures, and intellectual impairment. Two mutations ...
  7. ... found in a few people with features of myoclonic epilepsy with ragged-red fibers ... (ataxia), hearing loss, seizures, and diabetes.Mutations that cause ...
  8. ... is characterized by recurrent severe headaches, muscle weakness (myopathy), hearing ... movement (ataxia), and abnormal muscle cells known as ragged-red ...
  9. ... new mitochondrial transfer RNAPro gene mutation associated with myoclonic epilepsy with ... myopathy, deafness, and sporadic seizures associated with a novel ...
  10. ... TK gene have been identified in people with myoclonic epilepsy with ragged-red fibers (MERRF). This condition is ... MT-TK gene. Affected individuals may also have myopathy and ataxia. This mutation (written as G8363A) replaces the nucleotide ...
previous · 1 · 2 · next