The ZC4H2 gene plays a critical role in early neurological development, and mutations in this gene are associated with Wieacker-Wolff syndrome, a rare X-linked recessive disorder. This condition primarily affects males and is characterized by muscle weakness, developmental delays, and contractures, among other neurological and physical manifestations. Given the complexity and rarity of the syndrome, genetic testing for mutations in the ZC4H2 gene is a crucial tool for accurate diagnosis and understanding the condition's inheritance pattern within families.
DNA Labs UAE offers a specialized genetic test aimed at detecting mutations in the ZC4H2 gene to confirm the diagnosis of Wieacker-Wolff syndrome. The test involves analyzing the patient's DNA to identify specific mutations in the ZC4H2 gene that are known to cause the syndrome. This genetic test is an important step for affected families, as it aids in genetic counseling, management of the condition, and understanding the risk for future pregnancies.
The cost of the ZC4H2 Gene Wieacker-Wolff Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive analysis and the specialized expertise required to interpret the results accurately. For families facing the challenges of Wieacker-Wolff syndrome, this test provides essential information for managing the condition and planning for the future.
The PEX1 Gene Zellweger Syndrome Genetic Test is a specific diagnostic tool used to identify mutations in the PEX1 gene, which are associated with Zellweger Syndrome, a rare, inherited disorder characterized by the reduction or absence of functional peroxisomes in the cells of the body. This condition leads to a spectrum of medical issues, including abnormalities in the brain, liver, and kidneys, and difficulties in muscle tone and function. Early and accurate diagnosis through genetic testing is crucial for managing symptoms and improving the quality of life for affected individuals.
DNA Labs UAE offers this comprehensive genetic test for individuals suspected of having Zellweger Syndrome or for those with a family history of the condition. The test costs 4400 AED and involves analyzing the DNA for mutations in the PEX1 gene, which plays a significant role in the formation and function of peroxisomes. The procedure requires a simple blood sample from the patient, after which the sample is processed and analyzed in the laboratory.
The results from the PEX1 Gene Zellweger Syndrome Genetic Test can provide essential information for families and healthcare providers, enabling them to make informed decisions regarding treatment options and care plans. It also helps in understanding the risk of passing the condition to future generations, which is vital for affected families. DNA Labs UAE ensures confidentiality and accuracy in the testing process, offering support and guidance throughout the testing procedure.
The PEX12 Gene Zellweger Syndrome Genetic Test is a specialized diagnostic tool designed to identify mutations in the PEX12 gene, which are associated with Zellweger Syndrome, a rare genetic disorder. This condition is part of a spectrum of disorders known as peroxisome biogenesis disorders, characterized by impairments in the function of peroxisomes. These cellular organelles play a critical role in various metabolic processes, including the breakdown of fatty acids and the elimination of toxic substances.
Zellweger Syndrome manifests with a wide range of symptoms, including developmental delays, neurological issues, liver dysfunction, and distinctive facial features. Early diagnosis through genetic testing is crucial for managing symptoms and improving the quality of life for affected individuals.
The PEX12 Gene Zellweger Syndrome Genetic Test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing it for mutations in the PEX12 gene. The cost of the test is 4400 AED, reflecting the comprehensive analysis and expertise required to accurately identify the genetic variations associated with the syndrome.
By opting for this test, individuals at risk of carrying the genetic mutation or families with a history of Zellweger Syndrome can gain valuable insights into their genetic health, paving the way for early intervention and tailored medical care.
The PEX14 Gene Zellweger Syndrome Genetic Test is a specialized diagnostic tool designed to identify mutations in the PEX14 gene, which are linked to Zellweger Syndrome, a rare genetic disorder. This condition falls under the spectrum of peroxisome biogenesis disorders and is characterized by the impairment of multiple systems in the body, including the brain, liver, and kidneys. Early detection through genetic testing can provide crucial information for managing the syndrome, allowing for tailored treatments and interventions.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers a comprehensive analysis of the PEX14 gene to uncover any genetic abnormalities that could indicate the presence of Zellweger Syndrome. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed using advanced genetic sequencing techniques to identify mutations.
The cost of the PEX14 Gene Zellweger Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the intricate processes involved in genetic analysis and the specialized expertise required to interpret the results accurately. For families and individuals facing the possibility of Zellweger Syndrome, this test represents a critical step towards understanding the condition and planning for the necessary medical and supportive care.
The PEX16 Gene Zellweger Syndrome Genetic Test is a specialized diagnostic assessment designed to detect mutations in the PEX16 gene, which are associated with Zellweger Syndrome, a rare genetic disorder. This condition belongs to a group of diseases known as peroxisome biogenesis disorders, characterized by the body's inability to properly form peroxisomes, leading to severe metabolic complications. The PEX16 gene plays a crucial role in the formation of peroxisomes, and mutations in this gene can disrupt cellular processes, resulting in the symptoms observed in Zellweger Syndrome, which include developmental delays, neurological issues, and abnormalities in liver and kidney function.
Conducted at DNA Labs UAE, a leading genetic testing facility known for its advanced diagnostic technologies and expertise in genetic analysis, this test offers families and individuals critical information regarding the genetic underpinnings of Zellweger Syndrome. The test is priced at 4400 AED, reflecting the sophisticated nature of the genetic analysis and the specialized expertise required to interpret the results. Through a simple blood sample, the test aims to provide conclusive evidence of the presence or absence of mutations in the PEX16 gene, offering invaluable insights for affected families. This information can guide treatment decisions, inform family planning, and connect families with appropriate support and resources for managing the condition.
The PEX26 Gene Zellweger Syndrome Genetic Test is a specialized diagnostic tool used to detect mutations in the PEX26 gene, which is crucial for diagnosing Zellweger Syndrome, a rare, inherited disorder characterized by the absence or malfunction of peroxisomes in the cells of the body. This condition leads to a spectrum of medical issues, including impairments in the brain, liver, and kidneys, and affects physical and mental development.
The test is conducted by DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The procedure involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the lab to identify any genetic alterations in the PEX26 gene.
The cost of the PEX26 Gene Zellweger Syndrome Genetic Test is 4400 AED. This investment is crucial for families seeking answers to health questions related to Zellweger Syndrome, as early detection and understanding of the specific genetic mutation can guide treatment options, manage symptoms, and improve the quality of life for affected individuals.
The CYP17A1 gene plays a crucial role in the production of steroid hormones in the body, including cortisol, androgens, and estrogens. A deficiency in the 17-hydroxylation activity, governed by the CYP17A1 gene, can lead to a rare genetic condition that affects steroid hormone biosynthesis. This condition can manifest in various ways, including adrenal insufficiency and disorders of sex development, depending on the specific mutations in the CYP17A1 gene and the extent of enzyme activity impairment.
To diagnose this condition, a genetic test can be conducted to identify mutations in the CYP17A1 gene that are responsible for the deficiency in 17-hydroxylation activity. DNA Labs UAE offers this specialized genetic test, providing a crucial tool for the diagnosis and management of conditions arising from CYP17A1 gene mutations. The test is priced at 4400 AED and involves collecting a DNA sample from the patient, which is then analyzed for specific genetic mutations associated with the enzyme deficiency.
By accurately diagnosing the genetic basis of the condition, healthcare providers can tailor treatment and management plans to address the specific needs of the patient, potentially improving outcomes and quality of life for those affected by this rare genetic disorder.
The DECR1 Gene 24-Dienoyl-CoA Reductase 1 Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, aimed at identifying mutations in the DECR1 gene. This gene plays a critical role in the metabolism of very long-chain fatty acids by encoding an enzyme involved in the beta-oxidation pathway. Mutations in the DECR1 gene can lead to metabolic disorders that may impact an individual's health significantly.
The test is priced at 4400 AED and involves collecting a DNA sample from the patient, usually through a blood draw or cheek swab. The sample is then analyzed in the laboratory to detect any genetic variations in the DECR1 gene that may indicate a predisposition to related metabolic conditions. This genetic test is crucial for early diagnosis and management of potential metabolic issues, providing essential information for personalized treatment plans.
DNA Labs UAE, where this test is conducted, utilizes advanced genetic testing technologies to ensure accurate and reliable results. The test is recommended for individuals with a family history of metabolic disorders or those exhibiting symptoms related to abnormal fatty acid metabolism. By identifying genetic mutations early, patients can take proactive steps towards managing their health, guided by their healthcare provider's recommendations based on the test results.
The NADK2 Gene 24-Dienoyl-CoA Reductase Deficiency Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the NADK2 gene. This gene plays a crucial role in the metabolism of fatty acids and energy production within the body. Mutations in the NADK2 gene can lead to a rare metabolic disorder known as 24-Dienoyl-CoA Reductase Deficiency. This condition can result in a variety of symptoms, including developmental delays, muscle weakness, and metabolic crises, making early detection and management essential for affected individuals.
The test is performed using a blood sample from the patient, which is then analyzed using advanced genetic sequencing techniques to identify any mutations in the NADK2 gene. The cost of the test is 4400 AED, reflecting the comprehensive nature of the analysis and the specialized expertise required to interpret the results. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, this test offers a critical resource for families seeking answers to complex metabolic disorders. By identifying the genetic basis of the condition, the test can guide treatment decisions and provide valuable information for family planning.
The DHTKD1 Gene 2-Aminoadipic 2-Oxoadipic Aciduria Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE. This test is designed to identify mutations in the DHTKD1 gene, which have been associated with 2-Aminoadipic 2-Oxoadipic Aciduria, a rare metabolic disorder. The condition is characterized by the accumulation of certain compounds in the urine, leading to various metabolic issues. Individuals with this disorder may experience a range of symptoms, including developmental delay, muscle weakness, and potential neurological implications.
The test involves a detailed analysis of the DHTKD1 gene to pinpoint any genetic alterations that may contribute to the disorder. By identifying these mutations, healthcare providers can offer more accurate diagnoses, tailor treatment plans to the individual's genetic profile, and offer genetic counseling to families.
The cost of the DHTKD1 Gene 2-Aminoadipic 2-Oxoadipic Aciduria Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, which employs advanced genetic sequencing technologies to ensure accurate and reliable results. Conducting the test at DNA Labs UAE ensures that patients receive support from a team of genetic specialists and counselors, who can assist in interpreting the results and guiding subsequent steps for management or treatment of the condition.
