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MLYCD Gene Malonyl-CoA Decarboxylase Deficiency Genetic Test Cost
The MLYCD Gene Malonyl-CoA Decarboxylase Deficiency Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the MLYCD gene. These mutations are responsible for Malonyl-CoA decarboxylase deficiency, a rare genetic disorder that affects the body's ability to metabolize certain fats, leading to a buildup of malonic acid and other harmful substances. Symptoms of the disorder can vary but often include developmental delays, hypoglycemia, and cardiomyopathy, among others. The test, priced at 3200 AED, involves collecting a DNA sample from the patient, usually through a blood draw or a cheek swab. The sample is then analyzed in the laboratory using advanced genetic sequencing techniques to detect any abnormalities or mutations in the MLYCD gene. The results of this test can provide crucial information for the diagnosis and management of Malonyl-CoA decarboxylase deficiency, enabling targeted treatment plans and genetic counseling for affected families. DNA Labs UAE is equipped with state-of-the-art facilities and experienced professionals to ensure accurate and reliable testing outcomes.
MBL2 Gene Mannose-binding Protein Deficiency Genetic Test Cost
The MBL2 gene is responsible for encoding mannose-binding lectin (MBL), a protein that plays a crucial role in the innate immune system by binding to specific sugars on the surface of various microorganisms, thereby activating the complement system and aiding in the body's defense against infections. Deficiency in MBL due to mutations in the MBL2 gene can lead to an increased susceptibility to infections, particularly in young children, and may also have implications for autoimmune diseases. The MBL2 Gene Mannose-binding Protein Deficiency Genetic Test is a specialized diagnostic tool used to identify mutations in the MBL2 gene that lead to MBL deficiency. This test is critical for individuals who have recurrent infections without a clear cause, as it can confirm a deficiency in the mannose-binding lectin pathway, guiding appropriate management and treatment strategies to prevent further infections. The test is available at DNA Labs UAE, a leading facility in genetic diagnostics. The cost of the test is 4400 AED. Conducted in a state-of-the-art laboratory by experienced geneticists and technicians, the test involves analyzing the patient's DNA, extracted from a blood sample, for specific mutations in the MBL2 gene. Results from this test can provide valuable information for personalized medical care, enabling healthcare providers to make informed decisions about preventive measures, monitoring, and treatments tailored to the genetic makeup of the individual. DNA Labs UAE ensures confidentiality and accuracy in the testing process, with results typically available within a few weeks. The facility is equipped with advanced technology for genetic testing and analysis, providing patients and healthcare providers with reliable and comprehensive insights into MBL2 gene mutations and their potential impact on health.
MANBA Gene Mannosidosis-beta Genetic Test Cost
The MANBA Gene Mannosidosis-beta Genetic Test is a specialized diagnostic tool designed to identify mutations in the MANBA gene, which are associated with Beta-Mannosidosis - a rare inherited lysosomal storage disorder. This condition is characterized by a deficiency of the beta-mannosidase enzyme, leading to the accumulation of certain sugars in the body, which can result in a wide range of symptoms including developmental delay, hearing loss, recurrent infections, and skeletal abnormalities. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, to analyze the genetic sequence of the MANBA gene. This comprehensive analysis helps in confirming the diagnosis of Beta-Mannosidosis, understanding its severity, and informing potential treatment strategies. The cost of the MANBA Gene Mannosidosis-beta Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the intricate technologies and expert analysis required to accurately identify the specific gene mutations. Opting for this test can be a critical step for individuals showing symptoms of Beta-Mannosidosis or for those with a family history of the condition, aiming for early diagnosis and management of the disorder.
FXYD2 Gene Hypomagnesemia Type 2 Genetic Test Cost
The FXYD2 gene hypomagnesemia type 2 genetic test is a specialized diagnostic tool used to identify mutations in the FXYD2 gene, which are known to cause a specific type of inherited hypomagnesemia. Hypomagnesemia refers to abnormally low levels of magnesium in the blood, a condition that can lead to various health issues, including muscle weakness, seizures, and cardiac problems. Type 2 hypomagnesemia, linked to mutations in the FXYD2 gene, affects the kidney's ability to retain magnesium, leading to its excessive loss in urine. This genetic test involves analyzing the patient's DNA to detect any abnormalities in the FXYD2 gene that could be responsible for the condition. It is a critical step for families with a history of hypomagnesemia, offering them valuable insights into their genetic predispositions and aiding in the early diagnosis and management of the condition in affected family members. Performed at DNA Labs UAE, a leading facility in genetic testing, the test ensures high accuracy and reliability. The cost of the FXYD2 gene hypomagnesemia type 2 genetic test is set at 4400 AED. This investment covers the collection of the sample, usually a blood sample, the genetic analysis, and the comprehensive report detailing the findings. Given the specialized nature of this test and the profound implications of its results, it represents a critical tool in managing and understanding inherited hypomagnesemia, guiding both patients and healthcare providers in developing effective treatment and management plans.
CLDN16 Gene Hypomagnesemia Type 3 Genetic Test Cost
The CLDN16 Gene Hypomagnesemia Type 3 Genetic Test is a specialized diagnostic examination available at DNA Labs UAE, designed to identify mutations in the CLDN16 gene. These mutations are associated with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis (FHHNC) type 3, a rare inherited condition characterized by low levels of magnesium in the blood, increased levels of calcium in the urine, and the potential for kidney stone formation and renal impairment. This test is critical for individuals displaying symptoms of the disorder or those with a family history of FHHNC, as early detection can aid in managing symptoms and preventing severe kidney complications. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific genetic alterations in the CLDN16 gene. At DNA Labs UAE, the cost for the CLDN16 Gene Hypomagnesemia Type 3 Genetic Test is set at 4400 AED. This price reflects the comprehensive nature of the test, from the collection of the sample to the detailed genetic analysis and the provision of a conclusive report. The results from this test can provide invaluable information for affected individuals and their families, guiding treatment plans and informing about the risk of passing the condition on to future generations.
CNNM2 Gene Hypomagnesemia Type 6 Genetic Test Cost
The CNNM2 Gene Hypomagnesemia Type 6 Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to detect mutations in the CNNM2 gene, which are linked to Type 6 Hypomagnesemia. This condition is characterized by abnormally low levels of magnesium in the blood, a crucial mineral that plays a vital role in numerous bodily functions, including muscle and nerve function, bone health, and regulating blood pressure. Mutations in the CNNM2 gene can disrupt the body's ability to regulate magnesium levels properly, leading to a range of symptoms from muscle spasms and seizures to abnormal heart rhythms. The test is crucial for individuals showing symptoms of magnesium deficiency or those with a family history of Type 6 Hypomagnesemia, as early detection can significantly aid in managing the condition. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed for specific genetic alterations in the CNNM2 gene. The cost of the CNNM2 Gene Hypomagnesemia Type 6 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to identify the presence of any genetic mutations associated with the condition. Given the specialized nature of the test and the expertise required to interpret the results, the test price reflects the technical and professional services involved in providing accurate and actionable genetic insights.
ALPL Gene Hypophosphatasia Adult Genetic Test Cost
The ALPL Gene Hypophosphatasia Adult Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to identify mutations in the ALPL gene, which are indicative of hypophosphatasia (HPP) in adults. Hypophosphatasia is a rare, inherited disorder that affects bone mineralization, leading to a range of symptoms from mild dental issues to severe skeletal abnormalities. This genetic test is crucial for confirming the diagnosis, allowing for appropriate management and treatment strategies tailored to the individual's condition. The testing process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for specific mutations in the ALPL gene. The results can provide valuable information regarding the prognosis and guide healthcare professionals in making informed decisions regarding the patient's care. The cost of the ALPL Gene Hypophosphatasia Adult Genetic Test at DNA Labs UAE is set at 4400 AED. While the price may seem significant, the insights gained from this test can be invaluable for individuals showing symptoms of HPP, enabling early intervention and potentially improving quality of life. Patients interested in this test are encouraged to consult with their healthcare provider to discuss its relevance and implications based on their specific health condition and history.
ALPL Gene Hypophosphatasia Childhood Genetic Test Cost
The "ALPL Gene Hypophosphatasia Childhood Genetic Test" is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the ALPL gene, which are associated with hypophosphatasia (HPP) in children. Hypophosphatasia is a rare, inherited disorder that affects bone mineralization, leading to a range of symptoms from mild dental issues to severe skeletal abnormalities. The test specifically targets the ALPL gene, responsible for producing the enzyme alkaline phosphatase, critical for bone growth and maintenance. A mutation in this gene can result in reduced enzyme activity, leading to the symptoms associated with HPP. This genetic test is crucial for early diagnosis and management of the condition, allowing for targeted treatment strategies to improve quality of life and prevent severe complications. Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities, the test ensures high accuracy and reliability. The cost of the test is set at 4400 AED, reflecting the sophisticated nature of the genetic analysis and the comprehensive insight it provides into the patient's condition. Early diagnosis through this test can be a cornerstone in managing hypophosphatasia, offering affected children and their families hope for a better-managed condition.
