Symptoms and Testing information for GLDC Gene Glycine Encephalopathy Genetic Test

Symptoms and Testing information for GLDC Gene Glycine Encephalopathy Genetic Test

Glycine encephalopathy, also known as non-ketotic hyperglycinemia (NKH), is a rare genetic disorder affecting the body’s ability to break down the amino acid glycine. This condition results from mutations in several genes, including the GLDC gene. DNA Labs UAE offers a comprehensive genetic test for those concerned about this condition, providing essential insights into your genetic health.

Symptoms of GLDC Gene Glycine Encephalopathy

Glycine encephalopathy presents a range of symptoms, varying significantly from one individual to another. Early detection and understanding of these symptoms are crucial for managing the condition effectively. Common symptoms include:

  • Neurological Impairment: Affected individuals may experience seizures, hypotonia (reduced muscle tone), and lethargy due to the accumulation of glycine in the brain.
  • Developmental Delays: Children with glycine encephalopathy often face significant developmental challenges, including delays in reaching milestones such as walking and talking.
  • Breathing Difficulties: Some newborns with this condition may have breathing problems, including apnea, where breathing stops for short periods.
  • Feeding Difficulties: Difficulty feeding is common, which can lead to poor growth and development.
  • Intellectual Disability: Many individuals with glycine encephalopathy will have some degree of intellectual disability due to the impact of excess glycine on the brain.

It’s important to note that the severity of symptoms can vary widely. Some individuals may have mild symptoms, while others may experience life-threatening complications.

GLDC Gene Glycine Encephalopathy Genetic Test at DNA Labs UAE

DNA Labs UAE offers a genetic test specifically designed to identify mutations in the GLDC gene, which can lead to glycine encephalopathy. This test is a critical step for families with a history of the condition or for those who have children showing symptoms associated with glycine encephalopathy.

The test is priced at 4400 AED, reflecting the comprehensive analysis and detailed report provided. By identifying the specific mutations in the GLDC gene, our specialists can offer personalized advice on managing the condition, potential treatments, and the likelihood of passing the mutation on to future generations.

Understanding your genetic health is essential, and DNA Labs UAE is committed to providing accurate, confidential, and timely genetic testing services. For more information on the GLDC gene glycine encephalopathy genetic test and to schedule your test, please visit our website:

https://dnalabsuae.com/tests/gldc-gene-glycine-encephalopathy-genetic-test/

Conclusion

Glycine encephalopathy is a challenging condition, but early detection and understanding can significantly improve the quality of life for those affected. The GLDC gene glycine encephalopathy genetic test offered by DNA Labs UAE is a valuable resource for individuals and families seeking answers about this rare genetic disorder. With the right support and medical care, individuals with glycine encephalopathy can lead fulfilling lives.

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