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SUMF1 Gene Sulfatase deficiency Genetic Test Cost
The SUMF1 gene sulfatase deficiency genetic test is a specialized diagnostic procedure aimed at identifying mutations in the SUMF1 gene, which are associated with Multiple Sulfatase Deficiency (MSD). MSD is a rare genetic disorder that affects numerous bodily systems and leads to a wide range of symptoms, including developmental delays, skeletal abnormalities, and neurological issues. This condition is inherited in an autosomal recessive pattern, meaning that two copies of the mutated gene, one from each parent, are necessary for a child to be affected. The test is conducted through a blood sample, where DNA is extracted and analyzed for specific mutations in the SUMF1 gene that are known to cause the deficiency. It is a critical tool for confirming the diagnosis of MSD, allowing for appropriate management and counseling for affected families. Performed at DNA Labs UAE, the SUMF1 gene sulfatase deficiency genetic test is priced at 4400 AED. The facility ensures high-quality testing standards, providing reliable results for patients and healthcare providers. This test is essential for early diagnosis and intervention, potentially improving the quality of life for individuals with Multiple Sulfatase Deficiency.
SUOX Gene Sulfite oxidase deficiency Genetic Test Cost
The SUOX gene sulfite oxidase deficiency genetic test is a specialized diagnostic examination aimed at identifying mutations in the SUOX gene, which is responsible for coding the enzyme sulfite oxidase. This enzyme plays a crucial role in the metabolism of sulfur-containing amino acids. A deficiency in sulfite oxidase, due to mutations in the SUOX gene, can lead to a rare but serious disorder that affects the brain and other parts of the body. Symptoms of sulfite oxidase deficiency can range from severe neurological impairments to dislocated lenses and developmental delay, making early diagnosis critical for managing the condition. The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. By analyzing a patient's DNA, the test can identify specific mutations in the SUOX gene that are indicative of sulfite oxidase deficiency. This information is invaluable for clinicians in confirming a diagnosis, which can then guide treatment plans and inform family planning decisions. The cost of the SUOX gene sulfite oxidase deficiency genetic test at DNA Labs UAE is 4400 AED. While the price may seem significant, the test offers families and individuals critical insights into a condition that, if left undiagnosed, can lead to severe health complications. Early detection through genetic testing enables timely intervention and support, potentially improving the quality of life for those affected by sulfite oxidase deficiency.
SFTPD Gene Surfactant metabolism dysfunction Genetic Test Cost
The SFTPD gene plays a critical role in surfactant metabolism, which is crucial for lung function and respiratory health. Mutations in the SFTPD gene can lead to surfactant metabolism dysfunction, a condition that affects the lungs' ability to process and produce surfactant properly. Surfactant is a substance that prevents the collapse of alveoli (tiny air sacs in the lungs) and maintains proper lung function. To diagnose potential genetic issues related to surfactant metabolism dysfunction, a genetic test targeting the SFTPD gene can be conducted. This test examines the DNA sequence of the SFTPD gene to identify mutations that may be responsible for surfactant metabolism disorders. Early detection through genetic testing can be crucial in managing and treating conditions associated with surfactant dysfunction, potentially improving outcomes for affected individuals. In the UAE, DNA Labs offers the SFTPD Gene Surfactant Metabolism Dysfunction Genetic Test. The cost of this test is 4400 AED. DNA Labs UAE is known for its comprehensive genetic testing services, providing accurate and reliable results that can assist healthcare providers in diagnosing and managing genetic disorders related to surfactant metabolism. This test is an important tool for individuals with a family history of lung-related genetic disorders or for those exhibiting symptoms related to surfactant metabolism dysfunction, ensuring timely intervention and appropriate management of the condition.
UROS Gene Porphyria Congenital Erythropoietic Genetic Test Cost
The UROS Gene Porphyria Congenital Erythropoietic Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the UROS gene, which are responsible for Congenital Erythropoietic Porphyria (CEP). CEP is a rare genetic disorder that affects the body's ability to produce heme, an essential component of hemoglobin. This results in a buildup of porphyrins in the body, leading to severe photosensitivity, skin lesions, and potentially other systemic symptoms. Performed at DNA Labs UAE, this genetic test is pivotal for the accurate diagnosis of CEP, allowing for early intervention and management of the condition. The test involves collecting a DNA sample, typically through a blood draw, which is then analyzed for specific mutations in the UROS gene. The cost of the UROS Gene Porphyria Congenital Erythropoietic Genetic Test is 4400 AED. Given the complexity and the specialized nature of this test, it represents a critical step towards personalized medicine for individuals suspected of having this rare genetic disorder, offering them a clearer understanding of their condition and guiding treatment options.
PPOX Gene Porphyria Variegata Genetic Test Cost
The PPOX Gene Porphyria Variegata Genetic Test is a specific diagnostic tool used to identify mutations in the protoporphyrinogen oxidase (PPOX) gene, which are responsible for causing Porphyria Variegata (PV). This condition is a rare form of hepatic porphyria that leads to a deficiency in the enzyme protoporphyrinogen oxidase. This deficiency disrupts the heme production process, causing a buildup of porphyrins in the body, which can result in a range of symptoms including abdominal pain, skin photosensitivity, and neurological complications. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the patient's DNA to identify any genetic alterations in the PPOX gene. This precise genetic testing is crucial for confirming the diagnosis of Porphyria Variegata, enabling appropriate management and treatment of the condition. It also helps in identifying carriers of the gene mutation, which is vital information for affected families considering future pregnancies. The cost of the PPOX Gene Porphyria Variegata Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, from the initial collection of a DNA sample through to the detailed analysis and reporting by specialized geneticists. Given the complexity and the specialized technology required for this genetic testing, the cost is aligned with the high level of precision and reliability the test offers to patients and healthcare providers in diagnosing and managing Porphyria Variegata.
PEPD Gene Prolidase Deficiency Genetic Test Cost
The PEPD gene prolidase deficiency genetic test is a specialized diagnostic examination aimed at identifying mutations in the PEPD gene, which is responsible for encoding the enzyme prolidase. This enzyme plays a crucial role in the breakdown and recycling of proline and hydroxyproline, which are significant amino acids found in collagen. Prolidase deficiency is a rare metabolic disorder that can lead to a wide array of symptoms, including skin lesions, recurrent infections, intellectual disability, and skeletal abnormalities, among others. This genetic test involves analyzing the patient's DNA to detect any abnormalities or mutations in the PEPD gene that could lead to the enzyme's deficiency. It is a critical tool for confirming the diagnosis of prolidase deficiency, allowing for a better understanding of the condition's severity, potential complications, and guiding treatment options. The test is available at DNA Labs UAE, a leading facility in genetic testing and diagnostics. The cost of the PEPD gene prolidase deficiency genetic test at DNA Labs UAE is 4400 AED. This investment in testing is crucial for affected individuals and their families, as it provides essential information for managing the condition, planning for potential health issues, and understanding the risk for future generations.
PCCA Gene Propionic Acidemia Genetic Test Cost
The PCCA Gene Propionic Acidemia Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the PCCA gene, which are responsible for propionic acidemia. This rare genetic disorder disrupts the normal metabolism of certain parts of proteins and lipids, leading to the accumulation of propionic acid in the body. Symptoms can be severe and include poor feeding, vomiting, lethargy, and long-term health issues without prompt and proper treatment. The test is crucial for early detection, enabling targeted interventions and management strategies to mitigate the effects of the disorder. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific genetic mutations in the PCCA gene. Priced at 4400 AED, the test is an investment in health, offering invaluable information for affected individuals and their families. Early diagnosis through the PCCA Gene Propionic Acidemia Genetic Test at DNA Labs UAE can significantly improve the quality of life and outcomes for those with propionic acidemia, making it a critical tool in the management of this rare condition.
PCCB Gene Propionic Acidemia Genetic Test Cost
The PCCB Gene Propionic Acidemia Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, aimed at identifying mutations in the PCCB gene, which is known to cause propionic acidemia. Propionic acidemia is a rare, inherited metabolic disorder characterized by the inability of the body to process certain parts of proteins and lipids properly, leading to the accumulation of toxic substances in the body. This condition can lead to serious health issues, including developmental delay, intellectual disabilities, and physical health problems. The test is crucial for early detection and management of the condition, allowing for tailored treatment plans that can significantly improve the quality of life for affected individuals. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the PCCB gene. At DNA Labs UAE, the cost of the PCCB Gene Propionic Acidemia Genetic Test is set at 4400 AED. This investment covers the comprehensive analysis required to detect the genetic variations that cause propionic acidemia, providing essential information for affected families. Early diagnosis through this test can facilitate timely interventions, dietary management, and monitoring to mitigate the effects of the disorder, highlighting the test's value in the management of propionic acidemia.
