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COG5 Gene Glycosylation Disorder Type 2I Genetic Test Cost
The COG5 Gene Glycosylation Disorder Type 2I Genetic Test is a specialized diagnostic tool designed to identify mutations in the COG5 gene, which are associated with Congenital Disorders of Glycosylation (CDG). Type 2I CDG is a rare genetic condition that affects the normal process of adding sugar chains to proteins (glycosylation), crucial for various bodily functions. Symptoms of this disorder can range from mild to severe and may include developmental delay, neurological issues, and abnormalities in organ function. This genetic test involves analyzing the patient's DNA to detect specific mutations in the COG5 gene that are known to cause the disorder. Early diagnosis through this test can be pivotal in managing symptoms and improving the quality of life for affected individuals. The test is available at DNA Labs UAE, a leading facility in genetic diagnostics, ensuring high accuracy and reliability of results. The cost of the COG5 Gene Glycosylation Disorder Type 2I Genetic Test is set at 4400 AED. Given the complexity of the condition and the specialized nature of the test, this investment can be crucial for families seeking answers to unexplained symptoms related to glycosylation disorders.
COG4 Gene Glycosylation Disorder Type 2J Genetic Test Cost
The "COG4 Gene Glycosylation Disorder Type 2J Genetic Test" is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the COG4 gene, which are associated with a rare genetic disorder known as Congenital Disorders of Glycosylation Type IIj (CDG-IIj). This condition is part of a larger group of diseases that affect the normal process of adding sugar chains to proteins (glycosylation), which is crucial for proper protein function in various bodily processes. The COG4 gene plays a significant role in this glycosylation process, and mutations can lead to a wide range of symptoms, including developmental delay, neurological issues, and abnormalities in physical development. Early detection through this genetic test is vital for managing symptoms and improving the quality of life for affected individuals. 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 mutations in the COG4 gene. DNA Labs UAE employs advanced genetic sequencing techniques to ensure accurate and reliable results, providing crucial information for diagnosis, treatment planning, and genetic counseling for families affected by this disorder.
TMEM165 Gene Glycosylation Disorder Type 2K Genetic Test Cost
The TMEM165 Gene Glycosylation Disorder Type 2K Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the TMEM165 gene. These mutations are associated with Congenital Disorders of Glycosylation (CDG), specifically Type 2K, a rare genetic condition that affects the normal process of glycosylation - the addition of sugar molecules to proteins and lipids, which is crucial for their proper function. This disorder presents a spectrum of clinical manifestations, ranging from mild to severe, including developmental delay, neurological issues, and abnormalities in liver function, among others. Early and accurate diagnosis through genetic testing can be vital for the management and treatment of the condition, offering insights into potential therapies and interventions. The test is priced at 4400 AED and involves analyzing the patient's DNA sample to look for specific genetic alterations in the TMEM165 gene that are indicative of Type 2K CDG. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test adheres to the highest standards of accuracy and reliability, ensuring that patients receive precise and actionable genetic information.
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.
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.
