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GALK1 Gene Galactokinase deficiency Genetic Test Cost
The GALK1 gene is responsible for producing the enzyme galactokinase, which plays a crucial role in the metabolism of galactose, a type of sugar found in milk and other dairy products. Mutations in the GALK1 gene can lead to galactokinase deficiency, a rare genetic disorder that prevents the body from properly processing galactose. This condition can lead to various health issues, including cataracts, delayed growth, and learning difficulties if not managed properly. To diagnose this condition, a genetic test can be conducted to identify mutations in the GALK1 gene. DNA Labs UAE offers a comprehensive genetic test for galactokinase deficiency, providing a reliable means of diagnosis for those suspected of having the condition or carriers of the gene mutation. The test is priced at 3200 AED and involves analyzing the patient's DNA to detect any abnormalities in the GALK1 gene that could lead to the disorder. By opting for this test, individuals can gain crucial insights into their genetic health, enabling them to make informed decisions regarding their dietary intake and management of the condition.
GALE Gene Galactose epimerase deficiency Genetic Test Cost
The GALE Gene Galactose Epimerase Deficiency Genetic Test is a specialized diagnostic tool used to detect mutations in the GALE gene, which can lead to Galactose Epimerase Deficiency. This condition is a rare genetic disorder that affects the body's ability to process galactose, a sugar found in milk and other dairy products, leading to a range of metabolic issues. The test involves analyzing the patient's DNA to identify any genetic alterations in the GALE gene that could disrupt the normal metabolism of galactose. Performed at DNA Labs UAE, a leading facility in genetic testing, this test offers a critical resource for early diagnosis and management of Galactose Epimerase Deficiency. By identifying the condition early, healthcare providers can tailor dietary and medical interventions to prevent the serious health complications associated with the disorder. The cost of the GALE Gene Galactose Epimerase Deficiency Genetic Test is 4400 AED. While the price may seem significant, the test provides invaluable information for affected individuals and their families, enabling them to make informed decisions about health and treatment options.
SPINT2 Gene Diarrhea type 3 secretory sodium congenital syndromic Genetic Test Cost
The SPINT2 Gene Diarrhea Type 3 Secretory Sodium Congenital Syndromic Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE. This test specifically targets the analysis of the SPINT2 gene, which has been associated with a rare congenital disorder characterized by severe secretory diarrhea and various syndromic features. The condition, often referred to as Congenital Sodium Diarrhea (CSD), is a result of mutations in the SPINT2 gene that affect the body's ability to properly absorb and regulate sodium, leading to significant electrolyte imbalances and dehydration. The genetic test aims to identify mutations within the SPINT2 gene to confirm a diagnosis of this type of congenital diarrheal disorder. Early identification of the condition can significantly improve the management and treatment options for affected individuals, helping to mitigate some of the more severe symptoms and improve quality of life. The cost of the SPINT2 Gene Diarrhea Type 3 Secretory Sodium Congenital Syndromic Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test is conducted with state-of-the-art genetic sequencing technologies to ensure accurate and reliable results. Families who have a history of congenital diarrhea or syndromic features that may be linked to sodium imbalance are encouraged to consider this test for early detection and intervention.
NEUROG3 Gene Diarrhea type 4 malabsorptive congenital Genetic Test Cost
The "NEUROG3 Gene Diarrhea Type 4 Malabsorptive Congenital Genetic Test" is a specialized diagnostic tool designed to identify mutations in the NEUROG3 gene, which are associated with congenital malabsorptive diarrhea type 4. This condition is a rare genetic disorder characterized by severe diarrhea and an inability to properly absorb nutrients from food, often manifesting shortly after birth. The test is crucial for early diagnosis, allowing for appropriate management and treatment plans to be established, potentially improving the quality of life for affected individuals. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the patient's DNA to detect any abnormalities in the NEUROG3 gene. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology employed. By opting for this test, patients and their families can gain valuable insights into the genetic underpinnings of the condition, enabling informed decisions about care and support.
DPYD Gene Dihydropyrimidine dehydrogenase deficiency Genetic Test Cost
The DPYD gene dihydropyrimidine dehydrogenase deficiency genetic test is a specialized diagnostic tool designed to identify mutations in the DPYD gene, which is crucial for the proper metabolism of certain chemotherapy drugs, such as 5-fluorouracil (5-FU) and capecitabine. Individuals with a deficiency in the dihydropyrimidine dehydrogenase (DPD) enzyme, which is encoded by the DPYD gene, may experience severe or life-threatening toxicity when treated with these medications. The test aims to guide healthcare providers in customizing cancer treatment plans, ensuring the selection of safer and more effective chemotherapy options based on the patient's genetic makeup. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers a comprehensive analysis of the DPYD gene to detect any mutations that could indicate a risk of DPD deficiency. The cost of the test is set at 4400 AED, reflecting the intricate processes and sophisticated technology involved in providing accurate and reliable results. By identifying individuals at risk, the DPYD gene dihydropyrimidine dehydrogenase deficiency genetic test plays a critical role in personalized medicine, enhancing the safety and efficacy of cancer treatments.
DPYS Gene Dihydropyrimidinuria Genetic Test Cost
The DPYS gene dihydropyrimidinuria genetic test is a specialized diagnostic procedure designed to identify mutations in the DPYS gene, which are associated with dihydropyrimidinase deficiency. This condition affects the body's ability to break down certain components of proteins, leading to a buildup that can cause neurological issues, developmental delays, and other health problems. The test is crucial for early detection and management of the condition. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing a sample of the patient's DNA to look for specific mutations in the DPYS gene. This analysis helps in confirming the diagnosis of dihydropyrimidinase deficiency, enabling healthcare providers to tailor treatment and management plans for affected individuals. The cost of the DPYS gene dihydropyrimidinuria genetic test at DNA Labs UAE is set at 4400 AED. While the price might seem significant, the value of the information it provides for the medical management of individuals with dihydropyrimidinase deficiency cannot be understated. Early detection through this test can lead to interventions that significantly improve the quality of life for those affected by this rare genetic condition.
DMGDH Gene Dimethylglycine dehydrogenase deficiency Genetic Test Cost
The DMGDH gene is responsible for encoding the enzyme dimethylglycine dehydrogenase, which plays a crucial role in the metabolism of choline-derived compounds. Deficiency in this enzyme leads to a rare metabolic disorder characterized by elevated levels of dimethylglycine in the blood. This condition can result in a variety of symptoms, including developmental delays, muscular hypotonia, and in some cases, seizures. To diagnose this condition, a genetic test can be performed that specifically looks for mutations in the DMGDH gene. This test is critical for confirming the diagnosis, understanding the severity of the enzyme deficiency, and guiding treatment plans. It involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for mutations in the DMGDH gene. In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test for DMGDH gene deficiency. The cost of the test is 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by professionals with expertise in genetic testing, ensuring accurate and reliable results. This test is a valuable resource for families seeking answers to unexplained symptoms related to metabolic disorders and provides a foundation for personalized treatment strategies.
DYM Gene Dyggve-Melchior-Clausen disease Genetic Test Cost
The DYM gene Dyggve-Melchior-Clausen (DMC) disease genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the DYM gene, which are responsible for Dyggve-Melchior-Clausen disease. This rare genetic disorder is characterized by skeletal abnormalities, short trunk dwarfism, and, in some cases, developmental delays. The test plays a crucial role in the early detection and management of the condition, enabling healthcare providers to devise appropriate treatment and intervention strategies. Conducted in a state-of-the-art facility, the test ensures accuracy and reliability in results. The cost of the test is set at 4400 AED, reflecting the comprehensive nature of the analysis and the advanced technology employed in the testing process.