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AMPD3 Gene AMP Deaminase Deficiency Erythrocytic Genetic Test Cost
The AMPD3 Gene AMP Deaminase Deficiency Erythrocytic Genetic Test is a specialized diagnostic procedure designed to detect mutations in the AMPD3 gene, which can lead to AMP deaminase deficiency in erythrocytes (red blood cells). This condition is characterized by a reduced ability of red blood cells to metabolize adenosine monophosphate (AMP), which can lead to various hematological issues, including hemolytic anemia under certain stress conditions. The test involves analyzing the patient's DNA, extracted from a blood sample, to identify any genetic variations in the AMPD3 gene that are known to cause the deficiency. This is crucial for the accurate diagnosis and management of individuals with symptoms suggestive of this condition, as well as for genetic counseling of affected families. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability. The cost of the AMPD3 Gene AMP Deaminase Deficiency Erythrocytic Genetic Test is set at 4400 AED, reflecting the comprehensive analysis and detailed insights it provides into the patient's genetic makeup concerning the AMPD3 gene. This test is an essential tool for clinicians in diagnosing and managing patients with this rare genetic disorder, enabling personalized treatment plans and preventive measures for potential complications.
APOA1 Gene Amyloidosis Familial Visceral Genetic Test Cost
The "APOA1 Gene Amyloidosis Familial Visceral Genetic Test" is a specialized diagnostic tool designed to identify mutations in the APOA1 gene, which can lead to familial visceral amyloidosis. This condition is characterized by the abnormal deposition of amyloid proteins in organs and tissues, potentially leading to severe health complications. The APOA1 gene plays a crucial role in the production of Apolipoprotein A-I, a component of high-density lipoprotein (HDL), which is essential for lipid metabolism. Mutations in this gene can disrupt normal protein structure, leading to the formation of amyloid fibrils that accumulate in various body organs, such as the liver, kidneys, and heart, impairing their function. The test is available at DNA Labs UAE, a state-of-the-art facility known for its advanced genetic testing services. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and detailed insights it provides. By opting for this test, individuals with a family history of amyloidosis or those experiencing related symptoms can gain valuable information about their genetic predisposition to this condition. Early detection through this genetic test can be crucial in managing symptoms, preventing complications, and guiding treatment decisions, thereby enhancing the quality of life for affected individuals and their families.
GBE1 Gene Andersen Disease Genetic Test Cost
The GBE1 gene test is a genetic screening procedure aimed at identifying mutations in the GBE1 gene, which are associated with Andersen Disease, also known as Glycogen Storage Disease Type IV. This condition is a rare and often severe metabolic disorder that affects the body's ability to store and utilize glycogen, a key energy source. Mutations in the GBE1 gene lead to the abnormal functioning or deficiency of the glycogen branching enzyme, crucial for proper glycogen synthesis. As a result, an abnormal form of glycogen, known as polyglucosan, accumulates in tissues, particularly in the liver and muscles, causing various symptoms ranging from liver disease to muscle weakness, and in severe cases, it can be life-threatening. The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the GBE1 Gene Andersen Disease Genetic Test is 4400 AED. This test is particularly important for individuals with a family history of Andersen Disease or those exhibiting symptoms related to the disorder. Early detection through genetic testing can aid in the management of the disease, allowing for timely interventions and potentially improving the quality of life for those affected. DNA Labs UAE employs state-of-the-art technology and follows stringent protocols to ensure the accuracy and reliability of the test results, providing crucial information for patients and healthcare providers in diagnosing and managing Andersen Disease.
CDAN1 Gene Anemia Dyserythropoietic Type 1A Genetic Test Cost
The CDAN1 Gene Anemia Dyserythropoietic Type 1A Genetic Test is a specialized diagnostic tool designed to identify mutations in the CDAN1 gene, which are responsible for Congenital Dyserythropoietic Anemia Type 1A (CDA Type 1A). This rare genetic disorder affects the normal development of red blood cells, leading to anemia, jaundice, and, in some cases, an enlarged spleen and liver. Early and accurate diagnosis through this genetic test enables appropriate management and treatment strategies for affected individuals. The test involves collecting a DNA sample, typically through a blood draw, and analyzing it for specific genetic variations in the CDAN1 gene that are indicative of CDA Type 1A. This precise approach not only aids in confirming the diagnosis but also helps in distinguishing this type of anemia from other similar hematological conditions. Conducted at DNA Labs UAE, a facility renowned for its advanced genetic testing capabilities and stringent quality controls, the test ensures high accuracy and reliability. The cost of the CDAN1 Gene Anemia Dyserythropoietic Type 1A Genetic Test is set at 4400 AED, reflecting the sophisticated nature of the diagnostic procedure and the comprehensive analysis involved. Given the complexity of genetic disorders and the implications of a diagnosis, individuals undergoing this test can also benefit from genetic counseling services offered by DNA Labs UAE. This support is crucial for understanding the test results, the condition itself, and the potential impact on family planning and management options.
SEC23B Gene Anemia Dyserythropoietic Type 2 Genetic Test Cost
The SEC23B Gene Anemia Dyserythropoietic Type 2 Genetic Test is a specialized diagnostic tool used to identify mutations in the SEC23B gene, which are associated with Congenital Dyserythropoietic Anemia Type II (CDA II). This condition is a rare, inherited blood disorder characterized by ineffective erythropoiesis, leading to anemia, jaundice, and an enlarged spleen. The test is crucial for confirming the diagnosis, understanding the disease's progression, and making informed decisions regarding management and treatment options. Performed at DNA Labs UAE, the test involves collecting a blood sample from the patient and analyzing the genetic material for specific mutations in the SEC23B gene. This state-of-the-art facility ensures accurate and reliable results, providing essential information for patients and their families. The cost of the SEC23B Gene Anemia Dyserythropoietic Type 2 Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of a precise diagnosis cannot be underestimated, as it opens the door to targeted treatment plans and genetic counseling for affected families, potentially improving the quality of life for individuals with this rare condition.
SERPINA1 Gene Antitrypsin-alpha-1 deficiency Genetic Test Cost
The SERPINA1 gene encodes alpha-1 antitrypsin (AAT), a protein that plays a crucial role in protecting the lungs from inflammation caused by infection or irritants like tobacco smoke. Mutations in the SERPINA1 gene can lead to alpha-1 antitrypsin deficiency (AATD), a genetic condition that significantly increases the risk of lung and liver diseases. AATD is often underdiagnosed but can have serious implications for affected individuals. To diagnose AATD, a genetic test is conducted, targeting the SERPINA1 gene to identify any mutations. This test is crucial for individuals with a family history of AATD or related pulmonary conditions, as early detection can lead to interventions that significantly improve quality of life and health outcomes. In the United Arab Emirates, DNA Labs UAE offers this specific genetic test for AATD. The cost of the test is 4400 AED. The test involves a simple blood draw or buccal swab, after which the sample is analyzed in the lab for the presence of mutations in the SERPINA1 gene. Results from this test can provide individuals with valuable information about their genetic predisposition to AATD and guide both patients and healthcare providers in managing and potentially mitigating the impact of the condition.
HMGCS2 Gene 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency Genetic Test Cost
The HMGCS2 gene encodes the enzyme 3-hydroxy-3-methylglutaryl-CoA synthase 2, which plays a crucial role in the process of ketogenesis. This metabolic pathway occurs in the liver, converting fatty acids into ketone bodies, which serve as an essential energy source during prolonged fasting or carbohydrate restriction. A deficiency in the HMGCS2 enzyme can disrupt this process, leading to a range of metabolic issues and clinical symptoms, including hypoglycemia, lethargy, and in severe cases, neurological impairment. To diagnose this condition, a genetic test targeting the HMGCS2 gene can be conducted. This test specifically looks for mutations in the HMGCS2 gene that could lead to enzyme deficiency. It is a critical tool for confirming the diagnosis, enabling appropriate management and treatment strategies for affected individuals. In the UAE, this specific genetic test is available at DNA Labs UAE, a leading facility in genetic diagnostics. The cost of the HMGCS2 Gene 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency Genetic Test is 4400 AED. This test is instrumental for families with a history of metabolic disorders or for individuals presenting symptoms suggestive of HMGCS2 deficiency. Early detection through this genetic testing allows for timely intervention, potentially mitigating the severity of the condition's impact on the patient's health.
HADH Gene 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Genetic Test Cost
The HADH Gene 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, aimed at detecting mutations in the HADH gene. This gene plays a critical role in the metabolism of fatty acids within the body, and its mutations can lead to 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. This condition can result in a variety of metabolic problems, ranging from hypoglycemia to more severe metabolic crises. Early detection through this genetic test is crucial for the management and treatment of the condition, helping to prevent potential complications. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the presence of HADH gene mutations. By choosing DNA Labs UAE for this testing, patients can expect reliable results, which are essential for the subsequent management of the condition. DNA Labs UAE is known for its state-of-the-art facilities and highly qualified staff, ensuring that the testing process is both efficient and effective.
