Understanding the symptoms of DNMT1 Gene Neuropathy Sensor Type 1E is crucial for early detection and management of this condition. DNA Labs UAE offers a comprehensive genetic test designed to identify mutations in the DNMT1 gene, which are indicative of this specific neuropathy. The test is priced at 4400 AED, reflecting the intricate processes and […]
Neurology Diseases
Symptoms and Testing information for PMP22 Gene Neuropathy with Liability to Pressure Palsies HNPP Genetic Test
Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) is a genetic disorder that affects the peripheral nerves, which are responsible for sending signals between the brain and the muscles, as well as sensory information back to the brain. This condition is caused by mutations in the PMP22 gene, which plays a crucial role in the […]
Symptoms and Testing information for KIF2A Gene Neurodevelopmental Malformation and Microcephaly Genetic Test
At DNA Labs UAE, we are committed to providing advanced genetic testing to help diagnose a variety of genetic disorders, including those related to neurodevelopmental malformations and microcephaly. One of the critical genes associated with these conditions is the KIF2A gene. Understanding the symptoms associated with KIF2A gene mutations and the availability of genetic testing […]
Symptoms and Testing information for KIF5C Gene Neurodevelopmental Malformation and Microcephaly Genetic Test
Understanding the intricate nature of genetic conditions is pivotal in the realm of medical science. Among these conditions, neurodevelopmental disorders and microcephaly present significant challenges to affected individuals and their families. The KIF5C gene plays a crucial role in the normal development of the brain, and mutations in this gene can lead to severe neurodevelopmental […]
Symptoms and Testing information for GTPBP2 Gene Neurodegeneration with Brain Iron Accumulation GTPBP2 Related Genetic Test
Understanding the symptoms of GTPBP2 gene neurodegeneration with brain iron accumulation and the significance of GTPBP2 related genetic testing is crucial for early diagnosis and management of this condition. DNA Labs UAE offers a comprehensive genetic test for this purpose, priced at 4400 AED. This article delves into the symptoms associated with the disorder, the […]
Symptoms and Testing information for TUBG1 Gene Neurodevelopmental Malformation and Microcephaly Genetic Test
Symptoms of TUBG1 Gene Neurodevelopmental Malformation and Microcephaly Genetic Test Understanding the symptoms and genetic underpinnings of neurodevelopmental disorders is crucial for early diagnosis and intervention. One such condition, characterized by neurodevelopmental malformations and microcephaly, is linked to mutations in the TUBG1 gene. DNA Labs UAE offers a comprehensive genetic test to identify mutations in […]
Symptoms and Testing information for BRAT1 Gene Neurodevelopmental Disorder with Cerebellar Atrophy and with or Without Seizures Genetic Test
Understanding BRAT1 Gene Neurodevelopmental Disorder The BRAT1 gene neurodevelopmental disorder, also known as rigidity and multifocal seizure syndrome, neonatal onset, or early infantile epileptic encephalopathy 61, is a rare but severe condition that significantly impacts the central nervous system. This disorder is characterized by a range of symptoms, including cerebellar atrophy, which can lead to […]
Symptoms and Testing information for DES Gene Neurogenic Scapuloperoneal Syndrome Kaeser Type Genetic Test
DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide individuals with the most accurate and detailed genetic information. One of the specialized tests offered by DNA Labs UAE is the DES Gene Neurogenic Scapuloperoneal Syndrome Kaeser Type Genetic Test. This test is crucial for individuals […]
Symptoms and Testing information for ADAM22 Gene Neurodevelopmental Disorder ADAM22 Related Genetic Test
The ADAM22 gene plays a critical role in the development and function of the nervous system. Mutations or alterations in this gene can lead to a range of neurodevelopmental disorders, which may affect an individual’s cognitive, social, and motor skills. Recognizing the symptoms associated with ADAM22 gene neurodevelopmental disorder is crucial for early diagnosis and […]
Symptoms and Testing information for HINT1 Gene Neuromyotonia and Axonal Neuropathy Autosomal Recessive Genetic Test
Neuromyotonia and axonal neuropathy, also known as HINT1 neuropathy, is a rare genetic condition that affects the peripheral nervous system. This disorder is characterized by a range of symptoms that can significantly impact the quality of life of those affected. It is caused by mutations in the HINT1 gene and is inherited in an autosomal […]