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NARS2 Gene Combined oxidative phosphorylation deficiency type 24 Genetic Test Cost
The NARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 24 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE. This test is designed to identify mutations in the NARS2 gene, which have been associated with Combined Oxidative Phosphorylation Deficiency Type 24, a rare genetic disorder. This condition affects mitochondrial function, leading to a wide range of clinical manifestations, including developmental delay, muscle weakness, and neurological impairments. DNA Labs UAE offers this comprehensive genetic test for individuals who exhibit symptoms suggestive of mitochondrial disorders or have a family history of such conditions. The test involves analyzing the patient's DNA to detect mutations in the NARS2 gene, which are indicative of the disorder. Early detection through this test can be crucial for the management and treatment of the condition, potentially improving the quality of life for affected individuals. The cost of the NARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 24 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expertise required to accurately identify mutations in the NARS2 gene. Patients interested in this test are encouraged to consult with their healthcare provider to understand the benefits, implications, and process of genetic testing for diagnosing and managing mitochondrial disorders.
MARS2 Gene Combined oxidative phosphorylation deficiency type 25 Genetic Test Cost
The "MARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 25 Genetic Test" is a specialized diagnostic procedure available at DNA Labs UAE. This test specifically targets the MARS2 gene, which has been linked to Combined Oxidative Phosphorylation Deficiency 25 (COXPD25), a rare genetic disorder. COXPD25 is part of a group of conditions that affect the mitochondrial function, leading to a wide range of symptoms including neurological and muscular impairments, among others. The MARS2 gene plays a crucial role in mitochondrial protein synthesis, and mutations in this gene can disrupt the normal function of mitochondria, leading to the symptoms associated with COXPD25. The test is designed to identify mutations in the MARS2 gene, providing essential information for accurate diagnosis and management of the condition. It is particularly valuable for families with a history of mitochondrial disorders or unexplained symptoms consistent with mitochondrial dysfunction. Early diagnosis through genetic testing can facilitate timely intervention and management strategies to improve patient outcomes. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the MARS2 gene. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, patients can expect high-quality diagnostic processes guided by genetic experts. This test represents a crucial step forward in the personalized care and management of patients with suspected mitochondrial disorders, offering hope for better management of the condition.
MFSD8 Gene Ceroid lipofuscinosis neuronal type 7 Genetic Test Cost
The MFSD8 gene test for Ceroid Lipofuscinosis Neuronal Type 7 (CLN7) is a specialized genetic analysis offered by DNA Labs UAE. This test is designed to detect mutations in the MFSD8 gene, which are responsible for CLN7, a rare and severe neurodegenerative disorder that falls under the category of neuronal ceroid lipofuscinoses (NCLs). CLN7 is characterized by symptoms such as vision loss, cognitive decline, motor dysfunction, and seizures, typically manifesting in childhood. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the lab for specific genetic alterations in the MFSD8 gene. Identifying these mutations can confirm a diagnosis of CLN7, which is crucial for early intervention, management of symptoms, and genetic counseling for affected families. The cost of the MFSD8 gene test for Ceroid Lipofuscinosis Neuronal Type 7 at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to pinpoint the genetic mutations associated with this condition, providing essential information for affected individuals and their families regarding the diagnosis, prognosis, and potential treatment options.
CLN8 Gene Ceroid lipofuscinosis neuronal type 8 Genetic Test Cost
The CLN8 gene ceroid lipofuscinosis neuronal type 8 genetic test is a sophisticated diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the CLN8 gene, which are linked to a form of neuronal ceroid lipofuscinosis (NCL). NCLs are a group of progressive genetic disorders known as lysosomal storage diseases, which primarily affect the nervous system. Patients with mutations in the CLN8 gene typically exhibit symptoms such as seizures, visual impairment, cognitive decline, and motor dysfunction, with the severity and onset age varying among individuals. The test 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 in the CLN8 gene. This precise genetic testing can be crucial for early diagnosis, allowing for better management of the condition, genetic counseling, and informing family planning decisions. DNA Labs UAE offers this specialized genetic test for a cost of 4400 AED. The price reflects the intricate technology and expertise required to accurately identify mutations in the CLN8 gene and provide individuals and families with critical information about this rare genetic disorder. Early detection through this test can play a significant role in managing the symptoms and improving the quality of life for those affected by neuronal ceroid lipofuscinosis type 8.
ABHD5 Gene Chanarin-Dorfman syndrome Genetic Test Cost
The ABHD5 Gene Chanarin-Dorfman Syndrome Genetic Test is a sophisticated diagnostic tool available at DNA Labs UAE, designed to identify mutations in the ABHD5 gene, which are responsible for causing Chanarin-Dorfman Syndrome (CDS). This rare genetic disorder is characterized by the accumulation of lipids in various tissues of the body, leading to symptoms such as ichthyosis (scaly skin), liver enlargement, and occasionally hearing and vision problems. The test is particularly crucial for families with a history of the condition or individuals presenting symptoms suggestive of CDS. Priced at 4400 AED, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the state-of-the-art facilities at DNA Labs UAE. The laboratory employs advanced genetic sequencing technologies to scrutinize the ABHD5 gene for any mutations that could lead to the disorder. Results from this test can provide vital information for the diagnosis, management, and treatment planning of Chanarin-Dorfman Syndrome, offering affected individuals and their families a clearer understanding of the condition and how to best tackle it.
MT-RNR2 Gene Chloramphenicol resistance MT-RNR2 related Genetic Test Cost
The MT-RNR2 gene, also known as the mitochondrial ribosomal RNA 2 gene, plays a crucial role in the mitochondrial protein synthesis process. Mutations in this gene have been associated with various mitochondrial disorders and have implications for antibiotic resistance, particularly to chloramphenicol, an antibiotic used to treat bacterial infections. Chloramphenicol resistance can lead to treatment failure and necessitates alternative therapeutic strategies. The "MT-RNR2 Gene Chloramphenicol Resistance Genetic Test" is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the MT-RNR2 gene that could confer resistance to chloramphenicol. This test is particularly important for individuals with suspected mitochondrial disorders or in cases where there is a family history of chloramphenicol resistance. By determining the presence of specific genetic mutations, healthcare providers can make informed decisions about the use of chloramphenicol in treatment plans, potentially opting for alternative antibiotics to avoid ineffective treatment and adverse reactions. The test is priced at 3200 AED and involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory using advanced genetic testing techniques. Results from the test can help guide clinical decisions, contributing to personalized medicine and improved patient outcomes.
ABCB11 Gene Cholestasis benign recurrent intrahepatic type 2 Genetic Test Cost
The ABCB11 gene plays a crucial role in the body by coding for the bile salt export pump (BSEP), which is essential for the transport of bile acids from liver cells into the bile ducts. Mutations in the ABCB11 gene can lead to a condition known as benign recurrent intraheptic cholestasis type 2 (BRIC2), characterized by episodes of liver dysfunction that can cause jaundice, itching, and elevated liver enzymes. These episodes are typically not associated with long-term liver damage and tend to recur throughout life. To diagnose this condition, a genetic test targeting the ABCB11 gene can be performed. This test is particularly useful for individuals experiencing symptoms of cholestasis with no apparent cause, or for those with a family history of liver disorders. By analyzing the DNA for specific mutations in the ABCB11 gene, healthcare providers can confirm a diagnosis of BRIC2, which can significantly aid in the management and treatment of the condition. In the UAE, DNA Labs UAE offers this specialized genetic test for the ABCB11 gene. The cost of the test is 4400 AED. This test is conducted in a state-of-the-art laboratory setting by professionals who specialize in genetic analysis. The results from this test can provide valuable information for the patient and their healthcare provider, enabling a tailored approach to treatment and management of the condition, as well as offering insights into the prognosis and potential need for monitoring of liver function over time.
ABCB4 Gene Cholestasis intrahepatic of pregnancy type 3 Genetic Test Cost
The ABCB4 gene plays a crucial role in the proper function of the liver, particularly in the transportation of bile acids. Mutations in the ABCB4 gene can lead to a condition known as intrahepatic cholestasis of pregnancy (ICP) type 3, which is a liver disorder that occurs during pregnancy. This condition can cause severe itching and increase the risk of fetal distress, preterm birth, and stillbirth. Early diagnosis and management are essential for the health of both the mother and the fetus. The genetic test for ABCB4 gene cholestasis intrahepatic of pregnancy type 3 is a specialized diagnostic tool aimed at identifying mutations in the ABCB4 gene that are responsible for this condition. Conducted at DNA Labs UAE, this test provides crucial information for expecting mothers who may be at risk of developing ICP type 3. By detecting the specific genetic mutation, healthcare providers can tailor treatment and monitoring plans to manage symptoms effectively and reduce the risk of complications during pregnancy. The cost of the ABCB4 gene cholestasis intrahepatic of pregnancy type 3 genetic test at DNA Labs UAE is 3200 AED. This investment in prenatal care can significantly contribute to the well-being of both the mother and her unborn child by enabling early intervention strategies.