The RGS9 Gene Bradyopsia Genetic Test is a specialized diagnostic procedure designed to identify mutations in the RGS9 gene, which are responsible for the rare condition known as bradyopsia. Bradyopsia is characterized by a delayed adaptation of the eyes to changes in light, resulting in temporary blindness or impaired vision when transitioning between different lighting conditions. This condition affects the speed at which the retina can reset and respond to visual stimuli, leading to difficulties in activities that involve sudden changes in light, such as driving at night or entering a dimly lit room.
The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities in the RGS9 gene. Identifying these mutations can be crucial for understanding the cause of vision problems in affected individuals and can aid in the development of personalized management strategies to cope with the condition.
Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities and state-of-the-art technology, the RGS9 Gene Bradyopsia Genetic Test is priced at 4400 AED. DNA Labs UAE provides a comprehensive service, including pre-test counseling, sample collection, and detailed post-test analysis and advice, ensuring that patients receive not only accurate results but also the support and information they need to understand and manage their condition effectively.
The RGS9BP Gene Bradyopsia Genetic Test is a specialized genetic assessment conducted to diagnose bradyopsia, a rare inherited eye condition characterized by a delayed adaptation of the eyes to changes in light intensity. Individuals with bradyopsia experience difficulty adjusting from brightly lit environments to darker ones, or vice versa, which can significantly impact daily activities and quality of life. The condition is linked to mutations in the RGS9BP gene, which plays a crucial role in the visual phototransduction pathway.
This genetic test involves analyzing the patient's DNA to identify mutations in the RGS9BP gene that are responsible for bradyopsia. Early diagnosis through genetic testing can be crucial for managing symptoms and implementing strategies to cope with the visual impairment caused by this condition.
The test is available at DNA Labs UAE, a leading facility in genetic diagnostics and research. The cost of the RGS9BP Gene Bradyopsia Genetic Test is 4400 AED. This comprehensive testing service provides individuals and healthcare providers with critical information for the diagnosis and potential management of bradyopsia, enabling affected individuals to better understand their condition and live more comfortably with its implications.
The EYA1 gene test for Branchiootorenal Syndrome Type 1 is a specialized genetic test available at DNA Labs UAE. Priced at 4400 AED, this diagnostic tool is crucial for identifying mutations in the EYA1 gene, which are responsible for the development of Branchiootorenal Syndrome Type 1. This condition is characterized by an array of symptoms including branchial arch anomalies, hearing loss, and renal abnormalities. Early detection through this test can facilitate timely intervention and management of the syndrome. DNA Labs UAE employs state-of-the-art technology to ensure accurate and reliable results, aiding in the better understanding and treatment planning for affected individuals and their families.
The SIX5 Gene Branchiootorenal Syndrome Type 2 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the SIX5 gene, which are associated with Branchiootorenal Syndrome Type 2 (BOR2). BOR2 is a genetic condition characterized by developmental abnormalities affecting the ears, neck, and kidneys. Symptoms can vary widely among individuals but may include hearing loss, branchial cysts, renal anomalies, and other related issues.
This test is crucial for individuals with a family history of BOR2 or those exhibiting symptoms, as early diagnosis can lead to better management and treatment of the condition. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the lab for genetic mutations in the SIX5 gene.
At DNA Labs UAE, the cost for the SIX5 Gene Branchiootorenal Syndrome Type 2 Genetic Test is set at 4400 AED. The price reflects the sophisticated technology and expertise required to accurately identify mutations in the gene of interest. By opting for this test, patients gain crucial insights into their genetic makeup, empowering them with the knowledge to make informed decisions about their health and the management of BOR2.
The ZNF469 gene plays a crucial role in the structural integrity of the cornea, and mutations in this gene can lead to Brittle Cornea Syndrome (BCS), a rare genetic disorder characterized by thinning and increased fragility of the cornea that can lead to severe visual impairment. The ZNF469 Gene Brittle Cornea Syndrome Genetic Test is a specialized diagnostic tool designed to detect mutations in the ZNF469 gene, aiding in the diagnosis of BCS. This test is crucial for individuals with a family history of BCS or those exhibiting symptoms, as early diagnosis can lead to interventions that may preserve vision and prevent complications.
The test is available at DNA Labs UAE, a leading genetic testing facility known for its state-of-the-art technology and expertise in genetic diagnostics. The cost of the ZNF469 Gene Brittle Cornea Syndrome Genetic Test is 4400 AED. This investment covers the comprehensive analysis required to accurately identify the presence of ZNF469 gene mutations. Given the complexity and rarity of the condition, having access to such a targeted genetic test is invaluable for affected individuals and their families, offering them a clear path towards understanding their condition and exploring potential management strategies.
The "PITX3 Gene Cataract 11 Multiple Types Genetic Test" is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the PITX3 gene that are associated with Cataract 11, a condition characterized by multiple types of cataracts. Cataracts are a common eye condition where the lens of the eye becomes cloudy, leading to decreased vision. The PITX3 gene plays a crucial role in the development and maintenance of eye structures, and mutations in this gene can lead to various forms of congenital cataracts, which can be present at birth or develop during childhood.
This genetic test is essential for individuals with a family history of cataracts or early-onset cataracts, as it can provide a definitive diagnosis of the type of cataract linked to the PITX3 gene mutation. Early identification of the genetic cause can aid in better management and treatment planning for affected individuals. Moreover, the test can offer valuable information for families regarding the inheritance patterns and risk of passing the condition to future generations.
The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of mutations in the PITX3 gene. The cost of the test at DNA Labs UAE is 4400 AED, reflecting the specialized nature of the genetic analysis and the comprehensive information it provides. This investment can be invaluable for affected individuals and their families in understanding their condition and making informed health and lifestyle decisions.
The "CRYBB1 Gene Cataract Type 17 Multiple Types Genetic Test" is a specialized genetic analysis designed to detect mutations in the CRYBB1 gene, which have been associated with the development of Type 17 cataracts. These cataracts can manifest in various forms, impacting the eye's natural lens and potentially leading to impaired vision or blindness if left untreated. The test aims to identify individuals at risk, enabling early intervention and management strategies to preserve vision.
Administered at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, typically through a blood draw or a cheek swab. The sample is then analyzed for specific genetic variants in the CRYBB1 gene that are linked to the development of Type 17 cataracts. This genetic testing is crucial for families with a history of cataracts, offering insights into the risk of developing this condition and guiding decisions on monitoring and treatment options.
The cost of the "CRYBB1 Gene Cataract Type 17 Multiple Types Genetic Test" at DNA Labs UAE is 4400 AED. While the price may seem high, the value of early detection and the potential to take preventive measures or seek early treatment can be significant for those at risk. This test is an important tool in the field of ophthalmic genetics, providing individuals and families with critical information about their genetic predisposition to cataracts and helping healthcare professionals tailor care to each patient's unique genetic profile.
The CRYBA4 gene cataract type 23 genetic test is a specialized diagnostic procedure aimed at identifying mutations in the CRYBA4 gene, which are known to be associated with the development of a specific type of cataract, referred to as cataract type 23. This condition is characterized by the clouding of the eye's natural lens, leading to a decrease in vision and, if untreated, can result in blindness. The test is crucial for early detection, allowing for timely intervention and management strategies to preserve vision.
Performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test involves collecting a DNA sample from the patient, usually through a blood draw or a cheek swab. The sample is then analyzed using sophisticated genetic sequencing technologies to detect any mutations in the CRYBA4 gene.
The cost of the CRYBA4 gene cataract type 23 genetic test is set at 4400 AED. While the price may seem high, the value of early detection and the potential to prevent the progression of cataracts can be significant, not only in terms of maintaining quality of life but also in reducing the long-term healthcare costs associated with advanced cataract treatment or surgery.
Given the importance of genetic factors in the development of cataracts, this test is particularly recommended for individuals with a family history of the condition or those exhibiting early symptoms of cataracts. It provides a critical tool in the arsenal against vision impairment, offering hope for those at risk of this genetic form of cataract.
A Grandparent DNA Test is a specialized form of genetic testing designed to establish the biological relationship between grandparents and their grandchildren. This type of test is particularly useful in situations where a parent's direct DNA is not available for testing. By analyzing the DNA samples from grandparents and comparing them with the grandchild's DNA, experts can determine if there is a genetic match that confirms a biological relationship.
At DNA Labs UAE, the Grandparent DNA Test is meticulously conducted in a state-of-the-art laboratory setting by experienced geneticists. The test involves collecting DNA samples, usually through a non-invasive cheek swab from the grandparents and the grandchild. These samples are then analyzed using advanced genetic testing technologies to identify shared DNA sequences and markers that indicate a biological relationship.
The cost of a Grandparent DNA Test at DNA Labs UAE is set at 4800 AED. This fee encompasses the full testing process, from the collection of DNA samples to the detailed analysis and final reporting of results. Clients can expect a comprehensive and confidential service, ensuring accurate and reliable outcomes that can provide clarity on familial relationships.
DNA Labs UAE prides itself on its precision, confidentiality, and the ethical handling of all genetic testing services, making it a trusted choice for those seeking to establish biological family connections through a Grandparent DNA Test.
The Paternal Lineage Y-STR Test, available at DNA Labs UAE for a cost of 4800 AED, is a specialized genetic analysis designed to trace male lineage by examining specific markers on the Y chromosome known as Short Tandem Repeats (Y-STRs). This test is exclusively applicable to males, as only they possess a Y chromosome, inherited from their fathers. It is an invaluable tool for individuals seeking to understand their paternal ancestry, verify family relationships among males, or investigate paternal lineage in genealogical research. DNA Labs UAE employs cutting-edge genetic testing techniques to provide accurate and reliable results, making it an excellent choice for anyone looking to explore their paternal heritage.
