Symptoms and Testing information for MAT1A Gene Methionine Adenosyltransferase Deficiency Autosomal Recessive Genetic Test

Symptoms and Testing information for MAT1A Gene Methionine Adenosyltransferase Deficiency Autosomal Recessive Genetic Test

MAT1A gene methionine adenosyltransferase deficiency is a rare autosomal recessive genetic condition that can have significant health implications for those affected. Understanding the symptoms associated with this deficiency is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for this condition, which is priced at 4400 AED. For more information, visit [DNA Labs UAE](https://dnalabsuae.com/tests/mat1a-gene-methionine-adenosyltransferase-deficiency-autosomal-recessive-genetic-test/).

The MAT1A gene is responsible for the production of the enzyme methionine adenosyltransferase, which plays a vital role in the metabolism of methionine, an essential amino acid. Deficiency in this enzyme leads to a wide range of symptoms, primarily affecting the liver, muscles, and nervous system.

Symptoms of MAT1A Gene Methionine Adenosyltransferase Deficiency include:

1. Liver Dysfunction: Individuals may experience jaundice, hepatomegaly (enlarged liver), and in severe cases, liver failure. These symptoms result from the accumulation of methionine and its toxic metabolites, which the liver cannot process effectively.

2. Neurological Impairments: The deficiency can lead to developmental delays, intellectual disability, and muscle weakness. Some patients may also exhibit signs of peripheral neuropathy, such as numbness or tingling in the extremities.

3. Metabolic Complications: Affected individuals might show signs of metabolic acidosis, where the body produces too much acid or when the kidneys are not removing enough acid from the body. This can lead to a range of symptoms, including rapid breathing, confusion, and lethargy.

Early diagnosis and management of MAT1A gene methionine adenosyltransferase deficiency are essential to prevent the progression of symptoms and improve the quality of life for those affected. The genetic test offered by DNA Labs UAE for 4400 AED is a valuable tool in identifying this condition. It provides crucial information for the management and treatment of the deficiency.

For more details on the test and to understand how it can help in the diagnosis and management of MAT1A gene methionine adenosyltransferase deficiency, please visit [DNA Labs UAE](https://dnalabsuae.com/tests/mat1a-gene-methionine-adenosyltransferase-deficiency-autosomal-recessive-genetic-test/).

MAT1A gene methionine adenosyltransferase deficiency is a rare autosomal recessive genetic condition that can have significant health implications for those affected. Understanding the symptoms associated with this deficiency is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for this condition, which is priced at 4400 AED. For more information, visit DNA Labs UAE.

The MAT1A gene is responsible for the production of the enzyme methionine adenosyltransferase, which plays a vital role in the metabolism of methionine, an essential amino acid. Deficiency in this enzyme leads to a wide range of symptoms, primarily affecting the liver, muscles, and nervous system.

Symptoms of MAT1A Gene Methionine Adenosyltransferase Deficiency include:

  • Liver Dysfunction: Individuals may experience jaundice, hepatomegaly (enlarged liver), and in severe cases, liver failure. These symptoms result from the accumulation of methionine and its toxic metabolites, which the liver cannot process effectively.
  • Neurological Impairments: The deficiency can lead to developmental delays, intellectual disability, and muscle weakness. Some patients may also exhibit signs of peripheral neuropathy, such as numbness or tingling in the extremities.
  • Metabolic Complications: Affected individuals might show signs of metabolic acidosis, where the body produces too much acid or when the kidneys are not removing enough acid from the body. This can lead to a range of symptoms, including rapid breathing, confusion, and lethargy.

Early diagnosis and management of MAT1A gene methionine adenosyltransferase deficiency are essential to prevent the progression of symptoms and improve the quality of life for those affected. The genetic test offered by DNA Labs UAE for 4400 AED is a valuable tool in identifying this condition. It provides crucial information for the management and treatment of the deficiency.

For more details on the test and to understand how it can help in the diagnosis and management of MAT1A gene methionine adenosyltransferase deficiency, please visit DNA Labs UAE.

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