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PCK2 Gene Phosphoenolpyruvate Carboxykinase Deficiency Mitochondrial Genetic Test Cost
The PCK2 Gene Phosphoenolpyruvate Carboxykinase Deficiency Mitochondrial Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the PCK2 gene. This gene plays a critical role in the metabolic pathway that converts pyruvate to glucose, a process essential for maintaining normal blood sugar levels. Deficiencies in the PCK2 enzyme can lead to various metabolic disorders, making early detection and management crucial for affected individuals. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific genetic mutations in the PCK2 gene. This analysis helps in diagnosing the deficiency, understanding its severity, and planning appropriate treatment strategies. Priced at 4400 AED, the test is a valuable tool for individuals experiencing symptoms of metabolic disorders or those with a family history of such conditions, enabling timely intervention and management. DNA Labs UAE, with its state-of-the-art facilities and experienced professionals, ensures accurate and reliable testing, providing essential insights into the patient's metabolic health.
PHGDH Gene Phosphoglycerate Dehydrogenase Deficiency Genetic Test Cost
The PHGDH gene phosphoglycerate dehydrogenase deficiency genetic test is a specialized diagnostic tool designed to identify mutations in the PHGDH gene, which are responsible for phosphoglycerate dehydrogenase deficiency. This rare metabolic disorder affects the body's ability to break down and process amino acids properly, leading to a range of neurological symptoms and developmental delays. The test is crucial for confirming the diagnosis, allowing for appropriate management and treatment strategies to be implemented. Performed at DNA Labs UAE, a leading facility in genetic testing, this test ensures high accuracy and reliability. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and detailed reporting that accompanies this sophisticated diagnostic procedure.
SLC25A3 Gene Mitochondrial Phosphate Carrier Deficiency Genetic Test Cost
The SLC25A3 gene plays a crucial role in mitochondrial function, specifically in the transport of phosphate into the mitochondria, which is essential for energy production in cells. Mutations in the SLC25A3 gene can lead to mitochondrial phosphate carrier deficiency, a condition that can affect various systems in the body, leading to symptoms such as muscle weakness, respiratory problems, and developmental delays. To diagnose this genetic condition, DNA Labs UAE offers a specialized genetic test targeting the SLC25A3 gene. This test is designed to identify mutations in the SLC25A3 gene that could lead to mitochondrial phosphate carrier deficiency. The procedure involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities. The cost of the SLC25A3 gene mitochondrial phosphate carrier deficiency genetic test at DNA Labs UAE is 4400 AED. This price includes the cost of sample collection, genetic analysis, and a comprehensive report detailing the test results. The report will provide information on whether any mutations were found in the SLC25A3 gene and the potential implications for the individual's health. This test is crucial for individuals with a family history of mitochondrial disorders or those showing symptoms related to mitochondrial phosphate carrier deficiency, as it can provide valuable information for diagnosis and management of the condition.
MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test Cost
The MOCS1 Gene Molybdenum Cofactor Deficiency Type A Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the MOCS1 gene, which are linked to Molybdenum Cofactor Deficiency (MoCD) Type A. This rare, autosomal recessive metabolic disorder is characterized by the body's inability to produce molybdenum cofactor, essential for the function of certain enzymes. Symptoms can include severe neurological abnormalities, seizures, and developmental delays, often presenting shortly after birth. The test involves analyzing the patient's DNA to detect specific genetic mutations in the MOCS1 gene that cause the deficiency. Early and accurate diagnosis through this genetic test is crucial for managing symptoms and improving the quality of life, although treatment options are limited. The test is priced at 4400 AED and is conducted at DNA Labs UAE, a facility renowned for its state-of-the-art genetic testing services. By identifying carriers of the gene mutation, the test also serves as an important tool for genetic counseling and planning for families with a history of the disorder.
MOCS2 Gene Molybdenum Cofactor Deficiency Type B Genetic Test Cost
The MOCS2 gene plays a crucial role in the biosynthesis of the molybdenum cofactor, which is essential for the proper function of various enzymes in the body. Mutations in the MOCS2 gene can lead to Molybdenum Cofactor Deficiency Type B, a rare and severe metabolic disorder characterized by neurological damage, developmental delays, and often an early infantile death if not diagnosed and managed timely. DNA Labs UAE offers a genetic test specifically designed to detect mutations in the MOCS2 gene, providing crucial information for the diagnosis of Molybdenum Cofactor Deficiency Type B. This test is particularly important for families with a history of the disorder or those who have children exhibiting symptoms consistent with the deficiency. Early diagnosis through genetic testing can facilitate prompt management strategies that may improve outcomes. The cost of the MOCS2 Gene Molybdenum Cofactor Deficiency Type B Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to identify the presence of mutations in the MOCS2 gene, offering peace of mind and critical insights for affected families. Given the complexity and rarity of the condition, accessing this specialized genetic testing service can be an essential step in managing the disorder effectively.
GPHN Gene Molybdenum Cofactor Deficiency Type C Genetic Test Cost
The GPHN Gene Molybdenum Cofactor Deficiency Type C Genetic Test is a specialized diagnostic tool designed to identify mutations in the GPHN gene, which are responsible for Molybdenum Cofactor Deficiency (MoCD) Type C. MoCD is a rare, autosomal recessive metabolic disorder that affects the body's ability to process certain chemicals, leading to a buildup of toxic substances that can cause severe neurological damage and other symptoms. Early detection through genetic testing can be crucial for managing the condition and potentially mitigating its effects. This test is conducted by DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The process involves analyzing the patient's DNA sample, typically obtained through a blood draw or cheek swab, to look for specific mutations in the GPHN gene that are indicative of MoCD Type C. The results of this test can provide valuable information for families and healthcare providers, aiding in the diagnosis, treatment planning, and understanding of the condition's inheritance pattern. The cost of the GPHN Gene Molybdenum Cofactor Deficiency Type C Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to accurately identify mutations in the GPHN gene. While the cost may be a consideration for some families, the potential benefits of obtaining a definitive diagnosis and the guidance it can offer for managing the condition make it a valuable investment in the affected individual's health and well-being.
SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency Genetic Test Cost
The SLC16A1 gene encodes for Monocarboxylate Transporter 1 (MCT1), a crucial protein involved in the transport of lactate and other monocarboxylates across cell membranes, playing a vital role in cellular metabolism. A deficiency in this transporter, due to mutations in the SLC16A1 gene, can lead to various metabolic disorders, impacting the body's ability to process and utilize monocarboxylates effectively. The SLC16A1 Gene Monocarboxylate Transporter 1 Deficiency Genetic Test is a specialized diagnostic tool designed to identify mutations in the SLC16A1 gene that could lead to MCT1 deficiency. This test is particularly important for individuals presenting symptoms of metabolic disorders or for those with a family history of such conditions, as it can provide a definitive diagnosis and guide treatment and management strategies. Performed at DNA Labs UAE, a leading facility in genetic testing, this test offers a comprehensive analysis of the SLC16A1 gene. The cost of the test is set at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic variations associated with MCT1 deficiency. Through this test, patients and healthcare providers can gain crucial insights into the genetic basis of metabolic disorders, enabling personalized treatment plans and potentially improving patient outcomes.
GNPTAB Gene Mucolipidosis Type 2 Alphabeta Genetic Test Cost
The GNPTAB gene mucolipidosis type 2 alphabeta genetic test is a specialized diagnostic tool designed to identify mutations in the GNPTAB gene, which are responsible for mucolipidosis type II alphabeta (ML II alphabeta). This rare, inherited lysosomal storage disorder is characterized by skeletal abnormalities, developmental delay, and coarse facial features, among other symptoms. The condition results from the body's inability to properly break down and recycle certain materials within cells, due to deficiencies in the enzyme that the GNPTAB gene helps to produce. Conducted at DNA Labs UAE, this genetic test plays a crucial role in the early detection and management of mucolipidosis type II alphabeta. By analyzing a patient's DNA sample, the test can identify specific mutations in the GNPTAB gene, thereby confirming a diagnosis and facilitating early intervention strategies. This is particularly important for affected families in terms of genetic counseling and understanding the risk of recurrence in future pregnancies. The cost of the GNPTAB gene mucolipidosis type 2 alphabeta genetic test at DNA Labs UAE is 4400 AED. Given the complexity of the disorder and the specialized nature of the test, this price reflects the intricate processes involved in accurately identifying the genetic mutations associated with the condition. For families and individuals facing the possibility of mucolipidosis type II alphabeta, this test offers a vital step towards accurate diagnosis and the potential for tailored treatments and management plans to improve quality of life.
