The ADGRV1 gene, associated with familial type 4 febrile seizures, plays a crucial role in neurological functioning and its mutations have been linked to the occurrence of febrile seizures within families. These seizures are fever-induced convulsions that occur in children and are a symptom rather than a disease, often linked to genetic predispositions.
To identify the genetic underpinnings of this condition, the ADGRV1 Gene Febrile Seizures Familial Type 4 Genetic Test is offered by DNA Labs UAE. This specialized test aims to detect mutations in the ADGRV1 gene, providing crucial information for families with a history of febrile seizures. Understanding whether a child carries this mutation can help in managing and anticipating healthcare needs, as well as offering insights into the condition's hereditary nature.
The test is priced at 4400 AED, reflecting the comprehensive analysis and detailed insights it provides. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test ensures accuracy and reliability, offering families peace of mind and a pathway towards better-informed healthcare decisions.
The MED12 gene FG Syndrome Type 1 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, aimed at identifying mutations in the MED12 gene, which are associated with FG Syndrome Type 1. FG Syndrome is a rare genetic disorder that primarily affects males, leading to various developmental delays, intellectual disability, and physical anomalies. The test involves analyzing the patient's DNA to detect specific alterations in the MED12 gene that are indicative of this condition.
Priced at 4400 AED, the test is conducted under the guidance of genetic experts at DNA Labs UAE, employing state-of-the-art technology to ensure accurate and reliable results. This genetic test is crucial for early diagnosis, which can significantly aid in managing the symptoms of FG Syndrome Type 1 through tailored therapeutic strategies and interventions, enhancing the quality of life for affected individuals and their families.
The FLNA gene FG Syndrome Type 2 genetic test is a specialized diagnostic procedure aimed at identifying mutations in the FLNA gene, which are linked to FG Syndrome Type 2, a rare genetic disorder. This condition primarily affects males and can lead to a wide range of physical and developmental challenges, including intellectual disability, skeletal anomalies, and distinctive facial features. The test involves analyzing the patient's DNA to detect any abnormalities in the FLNA gene that may indicate the presence of the syndrome.
Conducted at DNA Labs UAE, a leading facility in genetic testing, this test offers a crucial step towards a definitive diagnosis, enabling healthcare providers to tailor treatment and management plans to the individual needs of the patient. The cost of the FLNA gene FG Syndrome Type 2 genetic test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the FLNA gene. By opting for this test, families and individuals gain valuable insights into their genetic health, paving the way for informed medical decisions and supportive care tailored to those with FG Syndrome Type 2.
The CASK Gene FG Syndrome Type 4 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the CASK gene, which are associated with FG Syndrome Type 4. This condition is a rare genetic disorder that affects various parts of the body, including the nervous system, leading to developmental delays, intellectual disability, and physical anomalies. The test is crucial for early detection and management of the syndrome, ensuring that individuals receive the appropriate care and interventions. Priced at 4400 AED, this test is a vital resource for families and healthcare providers seeking to understand the genetic underpinnings of FG Syndrome Type 4, facilitating personalized treatment plans and support for affected individuals.
The FLNC gene filaminopathy genetic test is a specialized diagnostic procedure designed to identify mutations in the FLNC gene, which can lead to a range of muscle-related disorders known as filaminopathies. These conditions are characterized by muscle weakness, structural heart problems, and in some cases, skeletal abnormalities. The FLNC gene plays a crucial role in the development and maintenance of the cellular cytoskeleton, thereby influencing muscle integrity and function.
Conducted at DNA Labs UAE, this test offers a comprehensive analysis of the FLNC gene to detect any genetic anomalies that may be responsible for filaminopathies. The procedure is crucial for individuals who exhibit symptoms of muscle disorders or have a family history of filaminopathies, as it can provide a definitive diagnosis, inform treatment options, and guide family planning decisions.
The cost of the FLNC gene filaminopathy genetic test is 4400 AED. This investment covers the technical processes involved in the genetic analysis, including the extraction of DNA, amplification, and sequencing of the FLNC gene, followed by a detailed interpretation of the results by genetic specialists. By opting for this test at DNA Labs UAE, patients gain access to cutting-edge genetic testing technology, expert analysis, and comprehensive support, ensuring accurate diagnosis and personalized care for those affected by filaminopathies.
The FMR1 Gene Fragile X Syndrome Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the FMR1 gene, which are indicative of Fragile X Syndrome (FXS). This condition is a genetic disorder that causes a range of developmental problems including learning disabilities and cognitive impairment. The test is particularly crucial for individuals with a family history of FXS or those showing symptoms of the disorder. By analyzing a sample of the individual's DNA, the test identifies variations in the CGG repeat length within the FMR1 gene, which are responsible for causing the syndrome. The cost of the FMR1 Gene Fragile X Syndrome Genetic Test at DNA Labs UAE is 4400 AED, making it a valuable resource for families seeking answers about this inheritable condition. Early diagnosis through this test can lead to better management and support for those affected by Fragile X Syndrome.
The FMR1 Gene Fragile X Tremor Ataxia Syndrome (FXTAS) Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the FMR1 gene. This gene is crucial because alterations in its structure are associated with Fragile X Tremor Ataxia Syndrome, a condition that affects the nervous system, leading to symptoms such as tremors, problems with movement and balance (ataxia), and cognitive impairments. The test is particularly important for individuals who have a family history of FXTAS or related disorders, as it can provide valuable information for managing and understanding the condition. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the FMR1 gene. Conducting this test at DNA Labs UAE ensures that patients receive reliable results, thanks to the lab's commitment to high-quality standards and its use of advanced genetic testing technologies.
The FXN Gene Friedreich Ataxia Genetic Test is a specialized diagnostic tool used to identify mutations in the FXN gene, which are responsible for Friedreich's ataxia, a rare inherited disease. This condition affects the nervous system and causes movement problems, and it can also lead to heart disease. The test is crucial for early diagnosis, which can aid in managing symptoms and planning for the necessary care and interventions.
Performed at DNA Labs UAE, the test involves analyzing a sample of the patient's DNA to look for specific genetic alterations associated with the condition. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the presence of the FXN gene mutations. This test is an important step for families with a history of Friedreich's ataxia, offering them crucial information for genetic counseling and decision-making regarding their health and future.
The FLNA Gene Frontometaphyseal Dysplasia Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the FLNA gene, which are responsible for Frontometaphyseal Dysplasia (FMD). FMD is a rare genetic disorder characterized by abnormalities in the development of the skeletal system and the muscles, leading to distinctive facial features, skeletal malformations, and other systemic complications. The FLNA gene plays a crucial role in cell structure and movement, and mutations in this gene can disrupt the normal development of bones and other tissues.
This genetic test involves analyzing the patient's DNA to detect mutations in the FLNA gene that are indicative of Frontometaphyseal Dysplasia. It is a critical tool for confirming a diagnosis of FMD, enabling appropriate medical management and genetic counseling for affected individuals and their families.
The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the FLNA Gene Frontometaphyseal Dysplasia Genetic Test is 4400 AED. This comprehensive test is conducted under stringent quality control measures to ensure accurate and reliable results, providing essential information for the diagnosis and management of Frontometaphyseal Dysplasia.
The FUCA1 Gene Fucosidosis Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the FUCA1 gene, which are responsible for the rare lysosomal storage disorder known as Fucosidosis. This condition is characterized by the body's inability to break down and eliminate fucose-containing substances due to a deficiency in the enzyme alpha-L-fucosidase, leading to a wide range of symptoms including developmental delay, growth retardation, and neurological deterioration.
Performed at DNA Labs UAE, this genetic test is a crucial tool for confirming the diagnosis of Fucosidosis, allowing for early intervention and management of the condition. The test involves analyzing the patient's DNA sample for specific mutations in the FUCA1 gene, providing insights into the severity of the enzyme deficiency and potential implications for the patient's health.
The cost of the FUCA1 Gene Fucosidosis Genetic Test at DNA Labs UAE is 4400 AED. This investment is essential for families seeking clarity on this genetic condition, enabling healthcare providers to tailor treatment and support strategies to improve the quality of life for individuals with Fucosidosis.
