Symptoms and Testing information for NGEF Gene Neurodevelopmental Disorder NGEF Related Genetic Test

Symptoms and Testing information for NGEF Gene Neurodevelopmental Disorder NGEF Related Genetic Test

The understanding of genetic factors contributing to neurodevelopmental disorders has significantly advanced in recent years. Among the genes of interest is the NGEF gene, mutations in which have been associated with a range of neurodevelopmental disorders. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including tests for the NGEF gene-related […]

Symptoms and Testing information for PIGQ Gene Neurodevelopmental Disorder PIGQ Related Genetic Test

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 KIF2A Gene Neurodevelopmental Malformation and Microcephaly Genetic Test

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

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

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 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

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 […]

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