The FOXL2 gene test is a specialized genetic analysis designed to diagnose conditions associated with mutations in the FOXL2 gene, notably Blepharophimosis, Epicanthus Inversus, and Ptosis (BPES). BPES is a rare genetic disorder that affects the development of the eyes and eyelids, leading to distinctive facial features. The condition is characterized by a narrowing of the eye opening (blepharophimosis), an inward folding of the skin of the upper eyelid (epicanthus inversus), and drooping of the upper eyelids (ptosis). In some cases, BPES can also impact ovarian function, leading to premature ovarian failure in women.
The FOXL2 gene test involves analyzing the patient's DNA to identify mutations in the FOXL2 gene, which plays a crucial role in eyelid and ovarian development. Identifying mutations in this gene can confirm a diagnosis of BPES, assist in understanding the risk of passing the condition to offspring, and guide management and treatment decisions.
In the United Arab Emirates, DNA Labs UAE offers this genetic test at a cost of 4400 AED. DNA Labs UAE is known for its advanced genetic testing services, providing accurate and reliable results. The test is conducted in a state-of-the-art laboratory by a team of specialized geneticists and healthcare professionals, ensuring high-quality standards and confidentiality of patient information.
The UBE3B Gene Blepharophimosis-Ptosis-Intellectual Disability Syndrome Genetic Test is a specialized diagnostic tool used to identify mutations in the UBE3B gene, which are linked to a rare genetic disorder. This condition is characterized by a combination of facial anomalies including blepharophimosis (a condition where the eyelids are horizontally shortened), ptosis (drooping of the upper eyelid), and intellectual disability among other possible features.
DNA Labs UAE offers this comprehensive genetic test to help in the diagnosis and management of individuals suspected of having this syndrome. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the UBE3B gene that are known to cause the disorder.
The cost of the UBE3B Gene Blepharophimosis-Ptosis-Intellectual Disability Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This investment can be crucial for affected families, providing them with a definitive diagnosis and enabling healthcare providers to tailor management and support strategies to the individual's needs, potentially improving quality of life and outcomes.
The RLBP1 Gene Bothnia Retinal Dystrophy Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the RLBP1 gene, which are associated with Bothnia Retinal Dystrophy. This genetic condition is a form of retinal dystrophy that predominantly affects vision, leading to symptoms such as night blindness and progressive loss of visual fields. Early and accurate diagnosis through genetic testing is crucial for the management and understanding of the condition, allowing affected individuals and their families to make informed decisions regarding treatment and lifestyle adjustments.
The test is priced at 4400 AED and involves collecting a DNA sample from the patient, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific genetic mutations in the RLBP1 gene. DNA Labs UAE, where this test is conducted, is equipped with state-of-the-art technology and staffed by experienced professionals to ensure accurate and reliable results.
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 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.
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.
