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Symptoms and Testing information for SETX Gene Ataxia-Oculomotor Apraxia Type 2 Genetic Test

Symptoms and Testing information for SETX Gene Ataxia-Oculomotor Apraxia Type 2 Genetic Test

At DNA Labs UAE, we understand the importance of accurate and reliable genetic testing for conditions like Ataxia-Oculomotor Apraxia Type 2 (AOA2), caused by mutations in the SETX gene. This rare condition is part of a group of disorders that affect the nervous system, leading to a progressive loss of muscle control and coordination. Recognizing […]

Symptoms and Testing information for APTX Gene Ataxia-Oculomotor Apraxia Type 1 Genetic Test

Symptoms and Testing information for APTX Gene Ataxia-Oculomotor Apraxia Type 1 Genetic Test

DNA Labs UAE is at the forefront of genetic testing and diagnostics, providing a comprehensive range of services designed to offer insights into various genetic conditions. Among these, the APTX Gene Ataxia-Oculomotor Apraxia Type 1 Genetic Test is a critical tool for individuals suspecting they might be affected by this rare but impactful genetic disorder. […]

Symptoms and Testing information for MT-TV Gene Ataxia Progressive Seizures Mental Deterioration and Hearing Loss MT-TV Related Genetic Test

Symptoms and Testing information for MT-TV Gene Ataxia Progressive Seizures Mental Deterioration and Hearing Loss MT-TV Related Genetic Test

Ataxia, progressive seizures, mental deterioration, and hearing loss represent a complex spectrum of symptoms that can significantly impact an individual’s quality of life. These symptoms can often be linked to genetic factors, one of which is mutations in the MT-TV gene. Understanding the implications of these mutations and the availability of genetic testing is crucial […]

Symptoms and Testing information for FLVCR1 Gene Ataxia Posterior Column with Retinitis Pigmentosa Genetic Test

Symptoms and Testing information for FLVCR1 Gene Ataxia Posterior Column with Retinitis Pigmentosa Genetic Test

Symptoms of FLVCR1 Gene Ataxia Posterior Column with Retinitis Pigmentosa Genetic Test Ataxia with posterior column involvement and retinitis pigmentosa is a rare, genetic, neurodegenerative disorder caused by mutations in the FLVCR1 gene. This condition presents a unique set of symptoms that significantly impact the lives of those affected. Understanding these symptoms is crucial for […]

Symptoms and Testing information for DNAJC3 Gene Ataxia Combined Cerebellar and Peripheral with Hearing Loss and Diabetes Mellitus Genetic Test

Symptoms and Testing information for DNAJC3 Gene Ataxia Combined Cerebellar and Peripheral with Hearing Loss and Diabetes Mellitus Genetic Test

DNA Labs UAE is at the forefront of genetic testing and personalized medicine, offering a wide range of services designed to provide individuals with critical information about their health and genetic predispositions. Among the numerous tests provided, the DNAJC3 Gene Ataxia Combined Cerebellar and Peripheral with Hearing Loss and Diabetes Mellitus Genetic Test is a […]

Symptoms and Testing information for COX20 Gene Ataxia and Muscle Hypotonia Genetic Test

Symptoms and Testing information for COX20 Gene Ataxia and Muscle Hypotonia Genetic Test

In the quest to understand and manage genetic disorders, the importance of accurate diagnosis cannot be overstated. One such condition that has garnered attention is the genetic disorder associated with the COX20 gene, which can lead to symptoms such as ataxia and muscle hypotonia. DNA Labs UAE is at the forefront of providing comprehensive genetic […]

Symptoms and Testing information for NLGN3 Gene Asperger syndrome susceptibility X-linked type 2 Genetic Test

Symptoms and Testing information for NLGN3 Gene Asperger syndrome susceptibility X-linked type 2 Genetic Test

Asperger syndrome, now considered part of the broader category of Autism Spectrum Disorder (ASD), is a complex and multifaceted condition that affects individuals differently. The identification of genetic markers associated with Asperger syndrome has been a significant step forward in understanding its complexities. Among these genetic markers, the NLGN3 gene plays a crucial role. DNA […]

Symptoms and Testing information for PRPS1 Gene Arts syndrome Genetic Test

Symptoms and Testing information for PRPS1 Gene Arts syndrome Genetic Test

Symptoms of PRPS1 Gene Arts Syndrome Genetic Test Arts Syndrome is a rare genetic disorder caused by mutations in the PRPS1 gene. This condition is characterized by a range of symptoms that affect multiple systems within the body. Recognizing the symptoms early on can lead to a timely diagnosis, which is crucial for managing the […]

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