What does MELAS mean in NEUROLOGY


Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a rare genetic disorder that affects the mitochondria, the energy-producing organelles of cells. MELAS is caused by mutations in mitochondrial DNA (mtDNA), which is inherited from the mother.

MELAS

MELAS meaning in Neurology in Medical

MELAS mostly used in an acronym Neurology in Category Medical that means Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes

Shorthand: MELAS,
Full Form: Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes

For more information of "Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes", see the section below.

» Medical » Neurology

Symptoms

The symptoms of MELAS can vary widely, but they often include:

  • Muscle weakness
  • Fatigue
  • Seizures
  • Stroke-like episodes
  • Vision problems
  • Hearing loss
  • Diabetes
  • Cardiac problems

Diagnosis

The diagnosis of MELAS is based on the patient's symptoms and a physical examination. Blood tests can be used to measure lactic acid levels, which are often elevated in MELAS. Genetic testing can be used to confirm the diagnosis.

Treatment

There is no cure for MELAS, but treatment can help to manage the symptoms. Treatment options include:

  • Medications to reduce lactic acid levels
  • Anticonvulsant medications to prevent seizures
  • Physical therapy to improve muscle strength
  • Speech therapy to improve communication

Conclusion

MELAS is a rare and debilitating disorder, but with treatment, many patients can live full and productive lives. If you think you or a loved one may have MELAS, it is important to see a doctor for diagnosis and treatment.

Essential Questions and Answers on Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes in "MEDICAL»NEUROLOGY"

What is MELAS?

MELAS is a rare mitochondrial disorder characterized by mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes. It is caused by mutations in mitochondrial DNA and affects the brain, muscles, and other organs.

What are the symptoms of MELAS?

Symptoms of MELAS can vary widely, but may include seizures, strokes, muscle weakness, vision problems, hearing loss, developmental delays, and cognitive impairment.

How is MELAS diagnosed?

MELAS is diagnosed through a combination of a thorough medical history, physical examination, blood tests, imaging studies, and genetic testing.

What is the treatment for MELAS?

There is no cure for MELAS, but treatments can help manage the symptoms and improve the quality of life. Treatments may include medications, physical therapy, occupational therapy, speech therapy, and dietary changes.

What is the prognosis for MELAS?

The prognosis for MELAS varies greatly depending on the severity of the symptoms. Some individuals may live a normal lifespan with minimal symptoms, while others may experience severe neurological and physical disabilities.

Is there a cure for MELAS?

Currently, there is no cure for MELAS. However, research is ongoing to develop new treatments and potentially a cure.

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