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SLC35A2 Gene Glycosylation Disorder Type 2M Genetic Test Cost
The SLC35A2 gene glycosylation disorder type 2M genetic test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the SLC35A2 gene. These mutations are responsible for a rare condition known as Congenital Disorder of Glycosylation Type IIm (CDG-IIm), which affects the body's ability to properly glycosylate proteins and lipids, crucial processes for normal cellular functions. The test, priced at 4400 AED, involves analyzing the patient's DNA to detect any abnormalities in the SLC35A2 gene that may lead to the disorder. This genetic testing is pivotal for early diagnosis and management of the condition, offering insights into potential treatments and interventions to improve the quality of life for affected individuals. DNA Labs UAE utilizes advanced genetic testing technologies to ensure accurate and reliable results for patients and their families seeking clarity on this complex genetic disorder.
COG6 Gene Glycosylation Disorder Type 3 Genetic Test Cost
The COG6 Gene Glycosylation Disorder Type 3 Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to identify mutations in the COG6 gene, which are implicated in causing a rare genetic disorder known as Congenital Disorders of Glycosylation Type IIj (CDG-IIj). This condition affects the normal process of glycosylation, an essential biological mechanism where sugars are attached to proteins and lipids, impacting various bodily functions and leading to a spectrum of clinical manifestations. These can range from mild to severe and may include developmental delay, liver dysfunction, coagulation abnormalities, and neurological issues, among others. The test, priced at 4400 AED, involves collecting a DNA sample, typically through a blood draw, which is then analyzed using advanced genetic sequencing technologies to detect any abnormalities or mutations in the COG6 gene. This precise genetic testing allows for an accurate diagnosis, enabling healthcare providers to tailor treatment and management plans to the specific needs of the patient. It also offers critical information for family planning and genetic counseling for families affected by this disorder. Given the complexity of Congenital Disorders of Glycosylation and the significant impact they can have on individuals and families, the COG6 Gene Glycosylation Disorder Type 3 Genetic Test represents a crucial step forward in understanding and managing this rare condition. DNA Labs UAE, with its commitment to providing cutting-edge genetic testing services, ensures that patients and their families have access to the necessary resources for accurate diagnosis and informed healthcare decisions.
DDOST Gene Glycosylation Disorder Type IR Genetic Test Cost
The "DDOST Gene Glycosylation Disorder Type IR Genetic Test" is a specialized diagnostic tool offered by DNA Labs UAE, aimed at identifying mutations in the DDOST gene. This gene plays a critical role in the process of glycosylation, which is essential for proper protein folding and function. Mutations in the DDOST gene can lead to Type IR Congenital Disorders of Glycosylation (CDG), a group of inherited conditions that affect multiple systems of the body, including the nervous system, immune system, and gastrointestinal system, among others. Symptoms of CDG can vary widely among individuals but may include developmental delay, intellectual disability, seizures, and problems with liver function. The test is priced at 4400 AED and involves collecting a DNA sample from the patient, usually through a blood draw or a cheek swab. The sample is then analyzed in the laboratory to detect any mutations in the DDOST gene that could indicate the presence of Type IR CDG. This genetic test is crucial for the accurate diagnosis of the disorder, which can, in turn, guide appropriate treatment and management strategies. DNA Labs UAE provides this testing service with a focus on accuracy, confidentiality, and support for patients and their families navigating the complexities of genetic disorders.
SSR4 Gene Glycosylation Disorder X-Linked Genetic Test Cost
The SSR4 Gene Glycosylation Disorder X-Linked Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, aimed at detecting abnormalities in the SSR4 gene, which can lead to a rare form of Congenital Disorders of Glycosylation (CDG). This condition, being X-linked, primarily affects males and can result in a wide range of symptoms including developmental delay, intellectual disabilities, and various organ system abnormalities. Glycosylation refers to the process by which sugars are chemically added to proteins or lipids, a crucial function for proper cellular and organ development. Mutations in the SSR4 gene disrupt this process, leading to the disorder. The test is priced at 4400 AED and involves a detailed analysis of the patient's DNA to identify any mutations in the SSR4 gene. Conducted at the state-of-the-art facilities of DNA Labs UAE, the test is designed for those who have a family history of the disorder or exhibit symptoms suggestive of a glycosylation disorder. By pinpointing the exact genetic anomaly, the test facilitates tailored treatment plans and allows for genetic counseling to assess the risk in future pregnancies. Given the complexity and rarity of the condition, this genetic test is a critical tool in the management and understanding of SSR4 Gene Glycosylation Disorder.
GLB1 Gene GM1-Gangliosidosis Type 1 Genetic Test Cost
The GLB1 Gene GM1-Gangliosidosis Type 1 Genetic Test is a specialized diagnostic tool used to detect mutations in the GLB1 gene, which are responsible for GM1-gangliosidosis type 1, a rare inherited lysosomal storage disorder. This condition is characterized by a wide spectrum of symptoms, ranging from severe neurological impairment to skeletal abnormalities, depending on the severity and type of mutation present. Early detection through this genetic test can be crucial for management and treatment options, potentially improving the quality of life for affected individuals. Performed at DNA Labs UAE, a leading facility in genetic testing, the test provides a comprehensive analysis of the GLB1 gene to identify specific mutations associated with the disease. The cost of the test is set at 4400 AED, reflecting the intricate processes involved in ensuring accurate and reliable results. By choosing DNA Labs UAE for this test, individuals can expect state-of-the-art technology and expertise, contributing to the early diagnosis and understanding of GM1-gangliosidosis type 1.
GLB1 Gene GM1-Gangliosidosis Type 2 Genetic Test Cost
The GLB1 gene GM1-Gangliosidosis Type 2 genetic test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the GLB1 gene responsible for GM1-gangliosidosis type 2. GM1-gangliosidosis is a rare inherited disorder that affects the body's ability to degrade certain lipids, leading to their accumulation in various tissues. This accumulation can result in symptoms ranging from skeletal abnormalities to severe neurological impairment. Type 2, also known as juvenile or late-infantile form, typically presents symptoms later in infancy and is characterized by a slower progression compared to the more severe infantile form. The test is conducted using a blood sample from the patient, where DNA is extracted and analyzed for specific mutations in the GLB1 gene that are known to cause the disorder. This genetic testing is crucial for accurate diagnosis, guiding treatment options, and providing information on the risk of passing the condition to future generations. At DNA Labs UAE, the cost for the GLB1 gene GM1-Gangliosidosis Type 2 genetic test is set at 4400 AED. Given the complexity of the disorder and the implications of the test results for patients and their families, the process is accompanied by comprehensive genetic counseling. This counseling ensures that individuals are fully informed about the implications of the test results, including understanding the nature of the disorder, the potential outcomes of the test, and the available support and treatment options.
HEXB Gene GM2-Gangliosidosis Type 2 Genetic Test Cost
The HEXB Gene GM2-Gangliosidosis Type 2 Genetic Test is a comprehensive diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the HEXB gene, which are responsible for the development of GM2-Gangliosidosis Type 2, also known as Sandhoff disease. This condition is a rare, inherited disorder characterized by the progressive destruction of nerve cells in the brain and spinal cord. The test aims to provide crucial information for early diagnosis and management of the disease, potentially guiding treatment options and genetic counseling for affected families. Performed using a sample of the patient's blood or saliva, the test examines the HEXB gene for specific mutations that lead to the enzyme deficiencies characteristic of Sandhoff disease. These enzyme deficiencies result in the accumulation of harmful substances, leading to the symptoms associated with the disorder. The cost of the HEXB Gene GM2-Gangliosidosis Type 2 Genetic Test at DNA Labs UAE is 4400 AED. Given the complexity of the condition and the specialized nature of the test, this price reflects the advanced technology and expertise required to accurately identify the genetic mutations associated with the disease. Patients seeking this test can expect a high level of accuracy and comprehensive support from DNA Labs UAE, making it a valuable resource for families facing the challenges of GM2-Gangliosidosis Type 2.
GAMT Gene Guanidinoacetate Methyltransferase Deficiency Genetic Test Cost
The GAMT (Guanidinoacetate Methyltransferase) Gene Deficiency Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE. This test is designed to identify mutations in the GAMT gene, which can lead to Guanidinoacetate Methyltransferase Deficiency - a rare disorder affecting the body's ability to produce creatine. Creatine is crucial for storing and utilizing energy, particularly in muscle and brain tissues. Individuals with this deficiency may experience a range of symptoms, including developmental delay, intellectual disability, and seizures. The test involves analyzing the patient's DNA to pinpoint any genetic alterations in the GAMT gene that may be causing the condition. This early and precise identification allows for a better understanding of the disorder, enabling tailored management and treatment plans that can significantly improve the quality of life for those affected. The cost of the GAMT Gene Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the specific genetic mutations associated with the condition, offering valuable insights for affected individuals and their families. With the expertise of DNA Labs UAE, patients can expect reliable and accurate results, facilitating informed decisions regarding their health and treatment options.