What does MELAS mean in THERAPY


MELAS is an acronym that stands for Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes. It is a rare genetic disorder that affects the mitochondria, which are the energy-producing organelles found in cells.

MELAS

MELAS meaning in Therapy in Medical

MELAS mostly used in an acronym Therapy 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.

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Symptoms

MELAS typically affects children or young adults and can cause a wide range of symptoms, including:

  • Neurological problems, such as seizures, strokes, developmental delays, and muscle weakness
  • Lactic acidosis, a buildup of lactic acid in the blood due to impaired mitochondrial function
  • Stroke-like episodes, which can cause temporary or permanent neurological deficits
  • Other symptoms, such as hearing loss, vision problems, cardiomyopathy, and diabetes

Causes

MELAS is caused by mutations in mitochondrial DNA (mtDNA), which is inherited from the mother. These mutations can affect the function of the mitochondria, leading to impaired energy production and the buildup of lactic acid in the body.

Diagnosis

MELAS is diagnosed based on a combination of clinical symptoms, family history, and genetic testing. Genetic testing can confirm the presence of mtDNA mutations that are associated with MELAS.

Treatment

There is no cure for MELAS, but treatment can help to manage the symptoms and improve quality of life. Treatment may include:

  • Medications to prevent seizures and strokes
  • Supplements to help reduce lactic acid buildup
  • Therapy to address muscle weakness and other neurological problems
  • Dietary modifications to avoid foods that can trigger symptoms

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

What is MELAS?

Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a rare genetic disorder that affects the mitochondria, the energy producers of the cells. It is characterized by episodes of stroke-like symptoms, seizures, muscle weakness, and difficulty speaking and understanding.

What causes MELAS?

MELAS is caused by mutations in the mitochondrial DNA, which is inherited from the mother. These mutations disrupt the function of the mitochondria, leading to a shortage of energy and the accumulation of lactic acid in the body.

What are the symptoms of MELAS?

The symptoms of MELAS can vary depending on the severity of the mutation. Common symptoms include:

  • Stroke-like episodes
  • Seizures
  • Muscle weakness
  • Difficulty speaking and understanding
  • Short stature
  • Hearing loss
  • Vision problems
  • Diabetes

How is MELAS diagnosed?

MELAS is diagnosed based on a combination of symptoms, a physical examination, and genetic testing. Genetic testing can identify mutations in the mitochondrial DNA that are associated with MELAS.

How is MELAS treated?

There is no cure for MELAS, but treatment can help to manage the symptoms and improve quality of life. Treatment may include:

  • Medications to prevent seizures and stroke-like episodes
  • Physical therapy to improve muscle strength
  • Speech therapy to improve communication skills
  • Dietary changes to reduce lactic acid production

What is the prognosis for MELAS?

The prognosis for MELAS varies depending on the severity of the mutation. Some people with MELAS may have a relatively mild condition, while others may have more severe symptoms that can be life-threatening.

Final Words: MELAS is a complex and challenging disorder that can have a significant impact on the lives of affected individuals and their families. Early diagnosis and appropriate management are essential for optimizing outcomes and improving quality of life. Ongoing research is focused on developing new therapies and treatments for MELAS and other mitochondrial disorders.

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