TGFBI Gene Corneal dystrophy epithelial basement membrane Genetic Test sale cost 4400 AED

TGFBI Gene Corneal dystrophy epithelial basement membrane Genetic Test Cost

The TGFBI Gene Corneal Dystrophy Epithelial Basement Membrane Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the TGFBI gene that are associated with various types of corneal dystrophies, including epithelial basement membrane dystrophy (EBMD). EBMD, also known as map-dot-fingerprint dystrophy, is a common eye condition that can lead to vision impairment due to irregularities in the cornea's epithelial basement membrane. The test plays a crucial role in the accurate diagnosis and management of patients affected by or at risk of developing this condition. By analyzing the patient's DNA, the test can pinpoint specific genetic mutations in the TGFBI gene, offering valuable insights into the disease's prognosis, potential treatment strategies, and the risk of inheritance for family members. The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to conduct this sophisticated genetic analysis. Conducted at DNA Labs UAE, a leading facility in genetic testing, this service ensures high accuracy and reliability, providing essential information for patients and healthcare providers in managing corneal dystrophies effectively.
SLC4A11 Gene Corneal endothelial dystrophy type 2 Genetic Test sale cost 4400 AED

SLC4A11 Gene Corneal endothelial dystrophy type 2 Genetic Test Cost

The SLC4A11 Gene Corneal Endothelial Dystrophy Type 2 Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, aimed at detecting mutations in the SLC4A11 gene, which are associated with the development of Corneal Endothelial Dystrophy Type 2 (CHED2). This condition is a rare, inherited eye disorder that primarily affects the endothelium, the innermost layer of the cornea, leading to swelling, blurred vision, and potentially severe visual impairment. The test is crucial for individuals with a family history of CHED2 or those exhibiting symptoms, as early detection can facilitate timely management and treatment options to preserve vision. Conducted through a blood sample or buccal swab, the test specifically looks for genetic abnormalities in the SLC4A11 gene, which plays a significant role in maintaining corneal transparency and hydration. Priced at 4400 AED, the genetic test at DNA Labs UAE is performed with high precision and accuracy, providing individuals and their healthcare providers with vital information for making informed decisions regarding the condition's management and treatment. The test not only aids in the diagnosis but also helps in understanding the risk of passing the condition to future generations, thereby playing a significant role in family planning and genetic counseling.
PXDN Gene Corneal opacification and other ocular anomalies Genetic Test sale cost 4400 AED

PXDN Gene Corneal opacification and other ocular anomalies Genetic Test Cost

The PXDN gene plays a crucial role in ocular development and function. Mutations in this gene have been linked to corneal opacification and various other ocular anomalies, which can impact vision quality and lead to significant visual impairment. To identify mutations in the PXDN gene that may contribute to these conditions, DNA Labs UAE offers a specialized genetic test. This genetic test involves analyzing the patient's DNA to detect any abnormalities or mutations in the PXDN gene that could be responsible for the development of corneal opacification and other related ocular anomalies. Early detection through this test can be crucial for the management and treatment of these conditions, offering a chance to mitigate the progression of symptoms and improve the patient's quality of life. The test is priced at 4400 AED and is conducted in DNA Labs UAE's state-of-the-art facilities. The lab employs cutting-edge technology and adheres to the highest standards of accuracy and reliability in genetic testing. Upon completion, a comprehensive report is provided, detailing the findings and, if applicable, recommendations for follow-up care or interventions. This test is an invaluable tool for individuals at risk of PXDN gene-related ocular conditions, enabling proactive healthcare decisions.
EFEMP1 Gene Doyne honeycob retinal dystrophy Genetic Test sale cost 4400 AED

EFEMP1 Gene Doyne honeycob retinal dystrophy Genetic Test Cost

The EFEMP1 gene test for Doyne honeycomb retinal dystrophy, offered by DNA Labs UAE, is a genetic screening aimed at detecting mutations in the EFEMP1 gene, which is associated with this specific form of retinal dystrophy. Doyne honeycomb retinal dystrophy, also known as Malattia Leventinese, is an inherited eye disorder characterized by the accumulation of drusen (yellow deposits) beneath the retina, leading to progressive vision loss. The test is crucial for individuals with a family history of the condition or those experiencing symptoms, providing valuable insights into their genetic predisposition. Performed at DNA Labs UAE, a facility known for its advanced genetic testing capabilities, the EFEMP1 gene test involves collecting a DNA sample, typically through a blood draw or cheek swab. The laboratory then analyzes the sample to identify any mutations in the EFEMP1 gene that could indicate the presence of or risk for developing Doyne honeycomb retinal dystrophy. The cost of the test is 4400 AED, reflecting the comprehensive analysis and the specialized technology employed in detecting the genetic markers associated with the condition. For patients and families, the results from this test can guide clinical decisions, including early intervention and management strategies, to preserve vision and improve quality of life. It also offers the chance for affected families to understand their risk of passing the condition onto future generations, aiding in informed family planning decisions.
CHN1 Gene Duane Retraction syndrome Genetic Test sale cost 4400 AED

CHN1 Gene Duane Retraction syndrome Genetic Test Cost

The CHN1 Gene Duane Retraction Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the CHN1 gene, which are associated with Duane Retraction Syndrome (DRS). DRS is a rare congenital eye movement disorder characterized by limited horizontal eye movement, retraction of the eyeball into the socket, and, in some cases, other abnormalities. This condition results from abnormal development of the eye muscles, with the CHN1 gene playing a critical role in this process. 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 anomalies in the CHN1 gene that might be responsible for the syndrome. This genetic testing is crucial for accurate diagnosis, helping in the management and treatment planning for individuals affected by DRS. It also offers valuable information for family planning to those who have a history of the syndrome in their family. At DNA Labs UAE, the CHN1 Gene Duane Retraction Syndrome Genetic Test is priced at 4400 AED. This cost encompasses the entire process, from sample collection to genetic analysis and the provision of results. By offering this test, DNA Labs UAE provides an essential service for the early and accurate diagnosis of Duane Retraction Syndrome, facilitating better outcomes for those affected by this genetic condition.
SALL4 Gene Duane Retraction syndrome Genetic Test sale cost 4400 AED

SALL4 Gene Duane Retraction syndrome Genetic Test Cost

The SALL4 Gene Duane Retraction Syndrome Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the SALL4 gene, which are linked to Duane Retraction Syndrome (DRS). This condition is a rare, congenital eye disorder characterized by limited horizontal eye movement, which often results in the retraction of the eyeball into the socket or other eye abnormalities. Early and accurate diagnosis through this genetic test allows for better management and understanding of the condition, potentially leading to more effective treatment plans and supportive care. The test involves a detailed analysis of the SALL4 gene to pinpoint specific genetic alterations responsible for the syndrome. It is a critical step for families seeking answers about the genetic underpinnings of DRS and its potential impact on their health and development. The cost of the SALL4 Gene Duane Retraction Syndrome Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive analysis required to accurately assess the presence of mutations in the SALL4 gene, providing essential insights for affected individuals and their families. The test is conducted in a state-of-the-art laboratory setting, ensuring high-quality standards and reliable results.
ADAR Gene Dyschromatosis symmetrica hereditaria Genetic Test sale cost 4400 AED

ADAR Gene Dyschromatosis symmetrica hereditaria Genetic Test Cost

The ADAR Gene Dyschromatosis Symmetrica Hereditaria Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the ADAR gene, which are known to cause Dyschromatosis Symmetrica Hereditaria (DSH). DSH is a rare genetic disorder characterized by a mixture of hyperpigmented and hypopigmented macules, primarily affecting the back of the hands and feet, and sometimes the face. These skin changes usually appear in early childhood and can vary significantly in pattern and extent among affected individuals. This genetic test is crucial for confirming a diagnosis of DSH, allowing for appropriate management and counseling. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the patient's DNA to detect mutations in the ADAR gene that are indicative of the condition. The process is thorough and is carried out by highly skilled professionals who ensure the accuracy and confidentiality of the results. The cost of the ADAR Gene Dyschromatosis Symmetrica Hereditaria Genetic Test at DNA Labs UAE is 4400 AED. While the price might seem steep, it reflects the sophisticated technology and expertise required to perform such a specialized test. For families and individuals facing the possibility of DSH, this test provides invaluable information that can guide decisions about treatment and management, as well as offer insights into the risk of passing the condition on to future generations.
FBN1 Gene Ectopia lentis familial Genetic Test sale cost 4400 AED

FBN1 Gene Ectopia lentis familial Genetic Test Cost

The FBN1 Gene Ectopia Lentis Familial Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the FBN1 gene, which are associated with familial ectopia lentis. Ectopia lentis is a condition characterized by the displacement or malposition of the eye's lens, which can lead to visual impairments. This condition is often hereditary and is linked to Marfan Syndrome and other connective tissue disorders, with the FBN1 gene playing a crucial role in the development of the body's connective tissues. This genetic test is critical for individuals with a family history of ectopia lentis or related connective tissue disorders, as early identification of FBN1 gene mutations can facilitate timely intervention and management of the condition. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed for specific mutations in the FBN1 gene that are known to cause ectopia lentis. DNA Labs UAE offers this comprehensive genetic test at a cost of 4400 AED. The test is conducted in a state-of-the-art laboratory setting by experienced geneticists and laboratory technicians, ensuring high accuracy and reliability of the results. By opting for this test, individuals can gain valuable insights into their genetic predisposition to ectopia lentis and related conditions, enabling them to make informed decisions about their health and future.
ADAMTSL4 Gene Ectopia lentis isolated autosomal recessive Genetic Test sale cost 4400 AED

ADAMTSL4 Gene Ectopia lentis isolated autosomal recessive Genetic Test Cost

The ADAMTSL4 gene ectopia lentis isolated autosomal recessive genetic test is a specialized diagnostic procedure designed to identify mutations in the ADAMTSL4 gene, which are known to cause isolated ectopia lentis in an autosomal recessive manner. Ectopia lentis refers to the dislocation or displacement of the eye's lens, a condition that can significantly affect vision. When caused by mutations in the ADAMTSL4 gene, the condition does not typically present with other systemic features, distinguishing it from syndromic forms of ectopia lentis. This genetic test involves analyzing the patient's DNA to detect mutations in the ADAMTSL4 gene that are responsible for the condition. Early detection through this test can aid in the management and treatment of ectopia lentis, helping to prevent potential complications and improve quality of life for affected individuals. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers a reliable and accurate means of diagnosis for families concerned about this inheritable eye condition. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the expertise required to interpret the results. By choosing DNA Labs UAE for this test, patients can expect high-quality service and comprehensive support throughout the testing process.
LOXL1 Gene Exfoliation syndrome susceptibility to Genetic Test sale cost 4400 AED

LOXL1 Gene Exfoliation syndrome susceptibility to Genetic Test Cost

The LOXL1 Gene Exfoliation Syndrome Susceptibility Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify genetic predispositions to exfoliation syndrome (XFS), a significant risk factor for glaucoma. This condition is characterized by the accumulation of extracellular fibrillar material in the eye, leading to increased intraocular pressure and potential vision loss. The LOXL1 gene has been identified as a critical factor in the development of XFS, making this test a crucial tool for early detection and management of the syndrome. The test involves analyzing the patient's DNA to detect mutations in the LOXL1 gene that are associated with an increased risk of developing exfoliation syndrome. Early identification of these genetic markers can enable proactive monitoring and intervention, potentially preserving vision by preventing the progression to glaucoma. Priced at 4400 AED, the LOXL1 Gene Exfoliation Syndrome Susceptibility Genetic Test is accessible at DNA Labs UAE, where cutting-edge technology and expertise ensure accurate and reliable results. Individuals with a family history of glaucoma or exfoliation syndrome, or those exhibiting early symptoms, may particularly benefit from this test, enabling them to take timely steps towards eye health management.
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