Neurology Diseases

Autism Spectrum Disorder (ASD) is a complex neurodevelopmental disorder characterized by a wide range of symptoms and levels of impairment. Genetic factors play a significant role in the development of ASD, and recent advances in genetic testing have made it possible to identify specific genetic markers associated with the disorder. One such marker is the […]

Autism Spectrum Disorder (ASD) is a complex neurodevelopmental disorder that affects communication, behavior, and social interactions. The cause of ASD is multifactorial, with genetics playing a significant role. One of the genes that has been linked to ASD is BPIFA3. Understanding the symptoms associated with BPIFA3 gene mutations and the availability of genetic testing can […]

Autism Spectrum Disorder (ASD) is a developmental disorder that affects communication and behavior. Although ASD can be diagnosed at any age, it is said to be a “developmental disorder” because symptoms generally appear in the first two years of life. Understanding the genetic components of ASD can help in early diagnosis and intervention, which are […]

Ataxia Telangiectasia Like Disorder (ATLD) is a rare, inherited condition that affects the nervous system, immune system, and other parts of the body. It is caused by mutations in the MRE11 gene, which plays a critical role in DNA repair processes. Individuals with ATLD often experience symptoms similar to those of Ataxia Telangiectasia (AT), although […]

Autism Spectrum Disorder (ASD) is a complex developmental condition that involves persistent challenges in social interaction, speech, nonverbal communication, and restricted/repetitive behaviors. The manifestations of ASD can vary significantly across individuals, but they typically appear in early childhood and affect a person’s ability to function socially across multiple settings, including home, school, and work. One […]

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 […]

Autism Spectrum Disorder (ASD) is a complex neurodevelopmental disorder that affects communication, behavior, and social interaction in varying degrees. The search for the underlying causes of ASD has led scientists to explore genetic factors that may contribute to the development of this condition. One such gene that has come under investigation is the MYO16 gene. […]

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 […]

The MXRA5 gene, also known as the Matrix-Remodeling Associated 5 gene, has been identified as a significant marker in the study of Autism Spectrum Disorder (ASD). Understanding the symptoms associated with MXRA5 gene mutations and the significance of genetic testing can provide invaluable insights for families and individuals navigating the complexities of autism. DNA Labs […]

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 […]