In the realm of genetic diagnostics and personalized medicine, understanding the intricacies of specific genetic disorders has become crucial for early detection, management, and, in some cases, prevention. Among these genetic conditions is the GARS1 Gene Neuronopathy, also known as Distal Hereditary Motor Type 5 (dHMN-V). This disorder, linked to mutations in the GARS1 gene, […]
Neurology Diseases
Symptoms and Testing information for IGHMBP2 Gene Neuronopathy Distal Hereditary Motor Type 6 Genetic Test
Distal Hereditary Motor Neuronopathy Type VI (dHMN-VI) is a rare genetic disorder that affects the peripheral nervous system, specifically targeting the motor neurons responsible for muscle control and movement. This condition is caused by mutations in the IGHMBP2 gene, which plays a crucial role in the development and maintenance of nerve cells. DNA Labs UAE […]
Symptoms and Testing information for PIGQ Gene Neurodevelopmental Disorder PIGQ Related Genetic Test
Neurodevelopmental disorders represent a broad category of conditions that typically manifest early in development and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. One such disorder is linked to mutations in the PIGQ gene, which is crucial for the proper development and function of the nervous system. Understanding […]
Symptoms and Testing information for TUBB Gene Neurodevelopmental Disorder TUBB Related Genetic Test
Symptoms of TUBB Gene Neurodevelopmental Disorder The TUBB gene plays a crucial role in the proper functioning and development of the human brain. Mutations in the TUBB gene can lead to a range of neurodevelopmental disorders, presenting a spectrum of symptoms that can significantly impact the quality of life. Understanding these symptoms is vital for […]
Symptoms and Testing information for ZNF311 Gene Neurodevelopmental Disorder ZNF311 Related Genetic Test
Understanding the intricacies of neurodevelopmental disorders is crucial in providing effective care and support for those affected. Among the myriad of genetic factors that contribute to these conditions, the ZNF311 gene has recently been identified as a significant player. Disorders linked to mutations in the ZNF311 gene are part of an emerging area of study, […]
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 […]