The "MAF Gene Cataract Pulverulent or Cerulean with or without Microcornea Genetic Test" is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the MAF gene, which are known to cause specific types of cataracts. These cataracts can appear as pulverulent (dusty or powdery) or cerulean (blue-dot) and may occur with or without microcornea, a condition where the cornea is abnormally small. The test is critical for individuals who exhibit symptoms of these eye conditions or have a family history of them, as early detection can aid in managing the disease and planning for potential treatments. The cost of the test is 4400 AED, reflecting the specialized nature of the genetic analysis and the sophisticated technology employed to ensure accurate results. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test represents a significant step forward in personalized medicine and offers hope for affected individuals and their families.
The NHS Gene Cataract X-Linked Genetic Test, available at DNA Labs UAE for a cost of 4400 AED, is a specialized diagnostic tool designed to identify mutations in the NHS gene, which are known to cause X-linked congenital cataracts. This type of cataract is inherited in an X-linked recessive pattern, predominantly affecting males, and is characterized by the clouding of the lens of the eye that is present from birth or develops shortly after. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities associated with this condition. Identifying these mutations can provide crucial information for families regarding the inheritance pattern, potential for recurrence in future generations, and options for genetic counseling. It is an invaluable resource for affected individuals and their families, offering insights into the genetic underpinnings of X-linked congenital cataracts and guiding decisions regarding management and treatment.
The GJA8 Gene Cataract-Microcornea Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the GJA8 gene, which are linked to the development of Cataract-Microcornea Syndrome. This genetic condition is characterized by the presence of cataracts along with microcornea, a condition where the cornea's diameter is less than 10 mm in both eyes, potentially leading to visual impairment.
The test is conducted through a detailed analysis of the patient's DNA to identify any genetic alterations in the GJA8 gene, which plays a crucial role in the development and maintenance of eye lens transparency and corneal size. Identifying mutations in this gene can help in confirming the diagnosis, understanding the risk of transmitting it to offspring, and potentially guiding treatment and management decisions for affected individuals.
At DNA Labs UAE, the cost of the GJA8 Gene Cataract-Microcornea Syndrome Genetic Test is set at 4400 AED. The test provides a crucial resource for families and individuals at risk of this genetic syndrome, offering insights that can lead to early intervention and personalized care plans to manage the condition effectively.
The "IARS2 Gene Cataracts Growth Hormone Deficiency Genetic Test" is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the IARS2 gene. Mutations in this gene are associated with a rare, inherited condition that can lead to the development of early-onset cataracts, growth hormone deficiency, and potentially other health issues. This test is crucial for individuals who exhibit symptoms related to these conditions or have a family history of similar genetic disorders. By analyzing the IARS2 gene, healthcare providers can confirm a diagnosis, allowing for early intervention and management of the condition. The test is priced at 4400 AED and is conducted in the state-of-the-art facilities of DNA Labs UAE, ensuring high-quality, reliable results for patients and their families.
The "CTC1 Gene Coat Plus Syndrome Genetic Test" is a specialized genetic screening designed to identify mutations in the CTC1 gene, which is closely associated with Coat Plus Syndrome. This syndrome is a rare genetic disorder characterized by a variety of symptoms including retinal dystrophy, intracranial calcifications, bone marrow failure, and others. The test plays a crucial role in the early diagnosis and management of the condition, allowing healthcare professionals to tailor treatments and interventions to the specific needs of the patient.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, this test is priced at 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in the field of genetic testing, ensuring accurate and reliable results. By opting for this test, patients and their families can gain invaluable insights into their genetic makeup, paving the way for informed healthcare decisions and personalized medical care.
The "WFS1 Gene Cataract Type 41 Genetic Test" is a specialized diagnostic procedure designed to detect mutations in the WFS1 gene, which are associated with Cataract Type 41, a specific form of cataract. This condition is characterized by the clouding of the eye's lens, leading to impaired vision. The test is crucial for individuals with a family history of this condition, as early detection can facilitate timely intervention and management strategies.
Performed at DNA Labs UAE, a leading facility in genetic testing, the test offers a comprehensive analysis of the WFS1 gene to identify any genetic anomalies that could predispose an individual to develop Cataract Type 41. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed using advanced genetic sequencing technologies.
The cost of the WFS1 Gene Cataract Type 41 Genetic Test at DNA Labs UAE is set at 4400 AED. While the price may seem steep, the value of the test lies in its ability to provide crucial information about an individual's genetic predisposition to cataracts, thereby allowing for early and more effective management of the condition.
The TYRP1 gene albinism oculocutaneous type 3 genetic test is a specialized diagnostic tool used to identify mutations in the TYRP1 gene, which are responsible for oculocutaneous albinism type 3 (OCA3), a form of albinism characterized by reduced melanin pigment in the hair, skin, and eyes. This condition can lead to visual problems and increased susceptibility to sun damage due to the lack of melanin. The test involves analyzing the patient's DNA to detect any abnormalities or mutations in the TYRP1 gene, providing crucial information for diagnosis, management, and genetic counseling.
The test is available at DNA Labs UAE, a leading facility in genetic testing and personalized medicine. The cost of the TYRP1 gene albinism oculocutaneous type 3 genetic test is 4400 AED. This investment covers the comprehensive process of collecting the sample, conducting the genetic analysis, and providing a detailed report on the findings. The results from this test can help in tailoring the management plan for individuals with OCA3, including strategies to protect the skin and eyes from sun exposure and addressing vision problems.
The C10ORF11 gene plays a critical role in the development of oculocutaneous albinism type 5 (OCA5), a rare genetic condition characterized by reduced pigmentation in the hair, skin, and eyes, and often accompanied by vision problems. OCA5 is a result of mutations in the C10ORF11 gene, which is involved in the biological pathways that produce melanin, the pigment responsible for color in these tissues.
DNA Labs UAE offers a specialized genetic test designed to identify mutations in the C10ORF11 gene, providing a definitive diagnosis for individuals suspected of having oculocutaneous albinism type 5. This test is crucial for early detection and management of the condition, which can help in addressing the vision problems and skin sensitivity to sunlight associated with OCA5.
The cost of the C10ORF11 gene albinism oculocutaneous type 5 genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the specific genetic alterations within the C10ORF11 gene that lead to the development of OCA5. By confirming the diagnosis, affected individuals and their families can gain a better understanding of the condition, leading to informed decisions about care and management.
The PAX6 Gene Aniridia Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the PAX6 gene, which are strongly associated with aniridia. Aniridia is a rare genetic disorder characterized by the partial or complete absence of the iris in the eye, leading to various visual impairments and potentially other ocular complications. The PAX6 gene plays a crucial role in eye development, and mutations in this gene can disrupt this process, resulting in aniridia or related eye conditions.
This test is particularly valuable for individuals who have a family history of aniridia or exhibit symptoms related to the condition, as it can provide definitive genetic evidence of the PAX6 mutation. Early identification of the mutation can aid in managing the disorder, guiding treatment options, and offering genetic counseling for affected families.
The cost of the PAX6 Gene Aniridia Genetic Test at DNA Labs UAE is set at 4400 AED. This investment includes the collection of a DNA sample, usually through a blood draw or cheek swab, and subsequent detailed analysis in the laboratory. The test results can offer crucial insights into the genetic underpinnings of aniridia, enabling healthcare providers to tailor their approach to the specific needs of the patient and their family.
The BEST1 gene bestrophinopathy genetic test is a specialized diagnostic tool used to detect mutations in the BEST1 gene, which are associated with a group of eye disorders known as bestrophinopathies. These disorders can lead to a range of visual impairments, including reduced vision, distorted vision, and in some cases, progressive loss of vision. The conditions linked to mutations in the BEST1 gene include Best vitelliform macular dystrophy, adult-onset vitelliform macular dystrophy, autosomal dominant vitreoretinochoroidopathy, and autosomal recessive bestrophinopathy.
This genetic test is performed to confirm a diagnosis, guide treatment plans, and provide information for family planning. It involves analyzing the patient's DNA to identify any mutations in the BEST1 gene that may be responsible for the development of bestrophinopathies.
The test is available at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the BEST1 gene bestrophinopathy genetic test is 4400 AED. This price may cover the collection of the sample, usually through a blood draw or cheek swab, the genetic analysis, and a detailed report explaining the results. It is advisable for patients to consult with a healthcare provider or a genetic counselor before and after undergoing genetic testing to understand the implications of the test results fully.
