ITPR1 Gene Gillespie syndrome Genetic Test sale cost 4400 AED

ITPR1 Gene Gillespie syndrome Genetic Test Cost

The ITPR1 gene Gillespie syndrome genetic test is a specialized diagnostic assessment offered at DNA Labs UAE, designed to detect mutations in the ITPR1 gene that are associated with Gillespie syndrome. Gillespie syndrome is a rare genetic disorder characterized by partial aniridia (absence of the iris), ataxia, and intellectual disability. The condition is inherited in an autosomal dominant manner, meaning a mutation in just one of the two copies of the gene is sufficient to cause the disorder. This test is critical for individuals who exhibit symptoms of Gillespie syndrome or have a family history of the condition, as it provides definitive genetic evidence of the ITPR1 gene mutation. Early and accurate diagnosis through this genetic test can facilitate appropriate management and interventions for affected individuals. The cost of the ITPR1 gene Gillespie syndrome genetic test at DNA Labs UAE is set at 4400 AED. This price reflects the comprehensive analysis involved in identifying the genetic mutation, including the collection of a DNA sample, typically through a blood draw or cheek swab, and the subsequent laboratory analysis. Once the test is completed, a detailed report is provided, outlining the findings and offering guidance for further steps. Given the specialized nature of this test and its importance in the diagnosis and management of Gillespie syndrome, it is a valuable tool for affected families. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experienced professionals to ensure accurate and reliable results.
ASB10 Gene Glaucoma open angle type 1F Genetic Test sale cost 4400 AED

ASB10 Gene Glaucoma open angle type 1F Genetic Test Cost

The ASB10 Gene Glaucoma Open Angle Type 1F Genetic Test is a specialized diagnostic tool designed to identify mutations in the ASB10 gene, which are implicated in the development of open-angle glaucoma type 1F. Open-angle glaucoma is the most common form of glaucoma, characterized by the gradual loss of vision due to damage to the optic nerve, often without early symptoms. The ASB10 gene plays a crucial role in eye health, and mutations in this gene can significantly increase the risk of developing this type of glaucoma. This genetic test is particularly important for individuals with a family history of glaucoma or those who are at an increased risk of developing the condition. Early identification of genetic predispositions allows for timely intervention and management strategies to prevent or slow down the progression of glaucoma, preserving vision. The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the ASB10 Gene Glaucoma Open Angle Type 1F Genetic Test is 4400 AED. 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 ASB10 gene. Results from this test can provide valuable information for personalized treatment plans and preventive measures for individuals at risk of developing open-angle glaucoma type 1F.
NTF4 Gene Glaucoma open angle type 1F Genetic Test sale cost 4400 AED

NTF4 Gene Glaucoma open angle type 1F Genetic Test Cost

The NTF4 Gene Glaucoma Open Angle Type 1F Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to detect mutations in the NTF4 gene, which have been associated with the development of open-angle glaucoma, specifically type 1F. Open-angle glaucoma is the most common form of glaucoma, characterized by the gradual loss of vision due to damage to the optic nerve, often without early symptoms. Mutations in the NTF4 gene can lead to reduced neurotrophin-4 protein levels, which is crucial for the survival of retinal ganglion cells. Identifying mutations in this gene can provide crucial information for the early detection and management of glaucoma, potentially preserving vision. The test is priced at 4400 AED and is conducted in the state-of-the-art facilities of DNA Labs UAE. The process 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 specific genetic mutations in the NTF4 gene. Results from this test can help healthcare providers develop a more personalized treatment plan for patients at risk of or diagnosed with open-angle glaucoma, focusing on early intervention and tailored management strategies to slow the progression of the disease.
WDR36 Gene Glaucoma open angle type 1G Genetic Test sale cost 4400 AED

WDR36 Gene Glaucoma open angle type 1G Genetic Test Cost

The WDR36 Gene Glaucoma Open Angle Type 1G Genetic Test is a specialized diagnostic assessment offered at DNA Labs UAE, designed to detect mutations in the WDR36 gene, which have been associated with open-angle glaucoma, the most common form of glaucoma. Open-angle glaucoma is characterized by the gradual loss of vision due to damage to the optic nerve, often without early symptoms, making genetic testing a valuable tool for early detection and management. The test is priced at 4400 AED and involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for specific genetic variations in the WDR36 gene that are known to increase the risk of developing open-angle glaucoma. Identifying individuals at risk allows for early intervention, potentially slowing the progression of the disease and preserving vision. DNA Labs UAE provides this testing service with a focus on accuracy, confidentiality, and support, offering a crucial resource for those with a family history of glaucoma or individuals experiencing related symptoms.
CYP1B1 Gene Glaucoma primary type 3A Genetic Test sale cost 4400 AED

CYP1B1 Gene Glaucoma primary type 3A Genetic Test Cost

The CYP1B1 Gene Glaucoma Primary Type 3A Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify mutations in the CYP1B1 gene that are associated with Primary Congenital Glaucoma (PCG), specifically type 3A. This form of glaucoma is a severe eye condition that typically presents itself in infancy or early childhood, leading to increased intraocular pressure, optic nerve damage, and potentially, loss of vision if left untreated. The CYP1B1 gene plays a critical role in the development of the eye's drainage system; mutations in this gene can disrupt this system, leading to the accumulation of eye fluid and increased pressure. The test is priced at 4400 AED and involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of genetic alterations in the CYP1B1 gene. Identifying these mutations can provide valuable information for the early diagnosis and management of glaucoma, allowing for timely intervention and a better prognosis for affected individuals. Additionally, this test can be useful for families with a history of Primary Congenital Glaucoma, offering them an opportunity for genetic counseling and informed decision-making regarding family planning. DNA Labs UAE utilizes advanced genetic testing technologies to ensure accurate and reliable results, contributing to the effective detection and management of glaucoma in susceptible individuals.
RB1 Gene Hereditary Retinoblastoma Genetic Test sale cost 4400 AED

RB1 Gene Hereditary Retinoblastoma Genetic Test Cost

The RB1 Gene Hereditary Retinoblastoma Genetic Test is a crucial diagnostic tool available at DNA Labs UAE, designed to identify mutations in the RB1 gene, which are strongly associated with hereditary retinoblastoma. Retinoblastoma is a rare form of eye cancer that predominantly affects young children and can be inherited. Early detection through this genetic testing can be life-saving and significantly influence the management and treatment options for affected individuals and their families. The test, priced at 4400 AED, involves analyzing the patient's DNA to look for abnormalities in the RB1 gene, which plays a critical role in cell cycle regulation and tumor suppression. By identifying specific mutations in this gene, healthcare providers can assess an individual's risk for developing retinoblastoma and implement appropriate surveillance and preventive measures. Conducted at DNA Labs UAE, a leading facility in genetic testing, the RB1 Gene Hereditary Retinoblastoma Genetic Test is performed under strict quality control measures, ensuring accurate and reliable results. The test not only aids in the early detection of retinoblastoma but also provides valuable information for family planning and the assessment of risk in siblings and future generations.
HPS4 Gene Hermansky Pudlak syndrome type 4 Genetic Test sale cost 4400 AED

HPS4 Gene Hermansky Pudlak syndrome type 4 Genetic Test Cost

The HPS4 gene Hermansky-Pudlak syndrome type 4 genetic test is a specialized diagnostic procedure aimed at identifying mutations in the HPS4 gene, which are responsible for causing Hermansky-Pudlak syndrome (HPS) type 4. This rare genetic disorder is characterized by a lack of pigmentation (albinism), bleeding disorders, and lung and bowel diseases. The test is crucial for early diagnosis, allowing for appropriate management and treatment of the condition. Performed 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, which is then analyzed for specific mutations in the HPS4 gene. The results can help in confirming the diagnosis, understanding the severity of the disorder, and informing patients and families about potential complications and the risk of passing the condition to future generations. The cost of the HPS4 gene Hermansky-Pudlak syndrome type 4 genetic test at DNA Labs UAE is 4400 AED. Given the complexity of the test and the specialized technology and expertise required to interpret the results accurately, the price reflects the comprehensive analysis and detailed report provided to patients or their healthcare providers. This test is an essential tool for individuals with a family history of HPS or related symptoms, guiding their healthcare decisions and improving their quality of life through tailored medical care.
HPS1 Gene Hermansky-Pudlak syndrome type 1 Genetic Test sale cost 4400 AED

HPS1 Gene Hermansky-Pudlak syndrome type 1 Genetic Test Cost

The HPS1 gene Hermansky-Pudlak syndrome type 1 genetic test is a specialized diagnostic tool used to identify mutations in the HPS1 gene, which are indicative of Hermansky-Pudlak syndrome type 1 (HPS1). HPS1 is a rare genetic disorder characterized by a lack of pigmentation (albinism), bleeding disorders, and lung and bowel diseases. It is caused by mutations in the HPS1 gene, which plays a crucial role in the formation and function of lysosomes and related organelles in cells. This genetic test is vital for the early diagnosis and management of HPS1, allowing for appropriate interventions and treatments to mitigate the symptoms and improve the quality of life for affected individuals. Early diagnosis can also provide valuable information for family planning and genetic counseling for families with a history of the disorder. The test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the expertise required to interpret the results accurately. DNA Labs UAE employs state-of-the-art technology and highly qualified professionals to ensure reliable and precise testing outcomes, making it a trusted choice for genetic diagnostics in the region.
AP3B1 Gene Hermansky-Pudlak syndrome type 2 Genetic Test sale cost 4400 AED

AP3B1 Gene Hermansky-Pudlak syndrome type 2 Genetic Test Cost

The AP3B1 gene plays a critical role in the development of Hermansky-Pudlak syndrome type 2 (HPS2), a rare genetic disorder characterized by albinism, bleeding disorders, and pulmonary and intestinal complications. The genetic test for HPS2 through the analysis of the AP3B1 gene is a pivotal step in diagnosing this condition, enabling healthcare professionals to devise appropriate management and treatment strategies for affected individuals. Conducted at DNA Labs UAE, the test scrutinizes the AP3B1 gene for mutations that lead to HPS2. This comprehensive genetic testing ensures a precise diagnosis, facilitating early intervention and tailored care plans for patients. The cost of the test is set at 4400 AED, reflecting the intricate processes and advanced technology utilized in identifying the genetic alterations associated with this syndrome. By opting for this genetic test, individuals suspected of having HPS2 or families with a history of the syndrome can gain valuable insights into their genetic makeup, paving the way for informed healthcare decisions and potentially mitigating the impact of the syndrome's symptoms. DNA Labs UAE, with its state-of-the-art facilities and expertise in genetic diagnostics, stands at the forefront of genetic testing services, offering hope and clarity to those affected by Hermansky-Pudlak syndrome type 2.
CACNA1F Gene Cone-rod dystrophy X-linked type 3 Genetic Test sale cost 4400 AED

CACNA1F Gene Cone-rod dystrophy X-linked type 3 Genetic Test Cost

The CACNA1F Gene Cone-rod dystrophy X-linked type 3 Genetic Test is a specialized diagnostic examination aimed at identifying mutations in the CACNA1F gene, which are associated with Cone-rod dystrophy X-linked type 3, a rare genetic disorder. This condition primarily affects the eyes, leading to a progressive loss of vision due to the deterioration of cone and rod cells in the retina. The test is crucial for early diagnosis, allowing for appropriate management and counseling for affected individuals and their families. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed for specific genetic alterations in the CACNA1F gene. The results can provide invaluable information for affected individuals, including insights into the progression of the disease, potential treatments, and the risk of passing the condition on to offspring. The cost of the CACNA1F Gene Cone-rod dystrophy X-linked type 3 Genetic Test is set at 4400 AED, reflecting the sophisticated technology and expert analysis required to accurately identify mutations in the CACNA1F gene. While the price may seem high, the information gained from this test can be critical for the effective management of Cone-rod dystrophy X-linked type 3, significantly impacting the quality of life for those diagnosed with this challenging condition.
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