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ATIC Gene AICA-Ribosiduria Due to ATIC Deficiency Genetic Test Cost
The "ATIC Gene AICA-Ribosiduria Due to ATIC Deficiency Genetic Test" is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the ATIC gene, which can lead to AICA-ribosiduria. This rare genetic disorder is characterized by an accumulation of AICA-riboside in bodily fluids and is caused by a deficiency in the ATIC enzyme, which plays a critical role in the purine biosynthesis pathway. Symptoms of the disorder may include developmental delay, physical disabilities, and neurological issues. This test is crucial for individuals who exhibit symptoms suggestive of AICA-ribosiduria or have a family history of the disorder, as early detection can aid in managing symptoms and improving the quality of life. The testing process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed for specific mutations in the ATIC gene that are known to cause the condition. The cost of the ATIC Gene AICA-Ribosiduria Due to ATIC Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to accurately identify the presence of the genetic mutation, providing essential information for diagnosis and potential treatment options. Given the specialized nature of this test and its importance in the diagnosis of a rare genetic disorder, the cost reflects the technical expertise and resources necessary to conduct the analysis and interpret the results.
HGD Gene Alkaptonuria Genetic Test Cost
The HGD Gene Alkaptonuria Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the HGD gene, which is responsible for alkaptonuria. Alkaptonuria is a rare inherited disorder that causes the body to be unable to properly break down certain amino acids, leading to a buildup of homogentisic acid in the body. This can result in darkening of the urine, arthritis, heart disease, and other complications. The test is crucial for early detection and management of the condition, allowing for interventions that can significantly improve the quality of life for those affected. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the HGD gene that are known to cause alkaptonuria. At DNA Labs UAE, the cost for the HGD Gene Alkaptonuria Genetic Test is set at 4400 AED. This price includes the full testing process, from sample collection to the comprehensive analysis and final report detailing the findings. It's important for individuals with a family history of alkaptonuria or those experiencing symptoms to consider this test, as early detection is key to managing the disease effectively.
A2M Gene Alpha-2-Macroglobulin Deficiency Genetic Test Cost
The A2M Gene Alpha-2-Macroglobulin Deficiency Genetic Test is a specialized diagnostic procedure designed to detect mutations in the A2M gene, which can lead to Alpha-2-Macroglobulin (A2M) deficiency. This condition is characterized by a lack of A2M, a vital plasma protein that plays a crucial role in the body's immune response and in protecting tissues from enzymes that could damage them. Identifying mutations in the A2M gene is essential for understanding the risk of developing related conditions, such as chronic obstructive pulmonary disease (COPD), liver cirrhosis, and certain types of cancer. Conducted at DNA Labs UAE, a leading facility in genetic testing, this test offers individuals the opportunity to gain insights into their genetic makeup, particularly concerning the A2M gene. The test is performed using a blood sample, from which DNA is extracted and analyzed for any abnormalities in the A2M gene. The cost of the A2M Gene Alpha-2-Macroglobulin Deficiency Genetic Test is 4400 AED. This price reflects the comprehensive nature of the test, including the advanced technology and expertise required to accurately identify mutations in the A2M gene. For individuals with a family history of conditions associated with A2M deficiency or those experiencing symptoms related to these conditions, this test provides a valuable tool for early detection and management, potentially improving health outcomes and quality of life.
OGDH Gene Alpha-Ketoglutarate Dehydrogenase Deficiency Genetic Test Cost
The OGDH gene plays a critical role in the body's energy production processes. It encodes for a subunit of the alpha-ketoglutarate dehydrogenase enzyme complex, which is pivotal in the Krebs cycle, a fundamental part of cellular respiration and energy production. Deficiencies in this enzyme can lead to a range of metabolic disorders, characterized by symptoms such as developmental delay, muscle weakness, and neurological issues. A genetic test for OGDH gene alpha-ketoglutarate dehydrogenase deficiency is a sophisticated diagnostic tool aimed at identifying mutations in the OGDH gene that could disrupt the function of the enzyme complex. This test is crucial for early detection and management of conditions associated with the deficiency, offering insights that can guide treatment and intervention strategies. In the UAE, this specific genetic test is available at DNA Labs, a state-of-the-art facility known for its comprehensive genetic testing services. The cost of the test is set at 3200 AED, reflecting the intricate processes and advanced technology involved in identifying the genetic variations associated with the deficiency. By opting for this test at DNA Labs UAE, individuals gain access to crucial genetic information, paving the way for personalized medical care tailored to their specific genetic makeup.
AMACR Gene Alpha-Methylacyl CoA Racemase Deficiency Genetic Test Cost
The AMACR gene, also known as Alpha-Methylacyl CoA Racemase, plays a crucial role in the metabolism of certain fatty acids and branched-chain amino acids. Deficiencies or mutations in this gene can lead to various metabolic disorders, including bile acid synthesis disorders and peroxisomal disorders, among others. These conditions can manifest with a range of symptoms, from mild to severe, affecting multiple organ systems. To diagnose conditions related to AMACR gene deficiencies, a genetic test is available at DNA Labs UAE. This test specifically looks for mutations in the AMACR gene that could lead to the aforementioned metabolic disorders. It is a critical tool for healthcare providers to accurately diagnose and manage these conditions effectively. The cost of the AMACR Gene Alpha-Methylacyl CoA Racemase Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This test is conducted using a sample of the patient's blood or saliva, and the procedure involves analyzing the DNA to identify any mutations in the AMACR gene. The results from this test can provide essential information for the diagnosis, treatment planning, and genetic counseling for affected individuals and their families.
ACY1 Gene Aminoacylase Deficiency Genetic Test Cost
The ACY1 Gene Aminoacylase Deficiency Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the ACY1 gene, which can lead to aminoacylase 1 deficiency. This rare genetic disorder disrupts the breakdown of specific amino acids, leading to a range of symptoms including neurological issues, developmental delays, and in some cases, metabolic complications. The test is critical for early diagnosis and management of the condition, enabling tailored treatment plans that can significantly improve the quality of life for affected individuals. Conducted through a comprehensive analysis of the patient's DNA, this test is priced at 4400 AED. It represents a vital step towards personalized medicine for patients with this rare genetic disorder, offering hope for better management of their condition.
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.