Symptoms of TIMM8A Gene Dystonia-Deafness Syndrome Genetic Test The TIMM8A gene dystonia-deafness syndrome, also known as Mohr-Tranebjaerg syndrome (MTS), is a rare X-linked recessive disorder characterized by a variety of symptoms. These symptoms primarily include dystonia, which is a movement disorder causing involuntary muscle contractions, and sensorineural deafness. Understanding the symptoms of this syndrome is […]
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Symptoms and Testing information for SPR Gene Dystonia DOPA-Responsive Autosomal Recessive Genetic Test
Understanding the genetic underpinnings of various diseases has been a significant advancement in medical science, providing insights into their diagnosis, management, and treatment. Among these, SPR Gene Dystonia, a DOPA-Responsive Autosomal Recessive disorder, stands out due to its unique characteristics and treatment responsiveness. DNA Labs UAE is at the forefront of diagnosing this condition through […]
Symptoms and Testing information for ACTB Gene Dystonia Juvenile-Onset Genetic Test
Understanding ACTB Gene Dystonia Juvenile-Onset Dystonia is a complex neurological condition characterized by involuntary muscle contractions, which can result in twisting and repetitive movements or abnormal postures. Juvenile-onset dystonia, which manifests in children and teenagers, can significantly impact the quality of life, making early diagnosis and management crucial. One of the genetic underpinnings of this […]
Symptoms and Testing information for HSPG2 Gene Dyssegmental Dysplasia Silverman-Handmaker Type Genetic Test
Dyssegmental Dysplasia, Silverman-Handmaker type, is a rare genetic disorder that affects the development of bones. It is caused by mutations in the HSPG2 gene. This condition is characterized by severe growth abnormalities, including short limbs and a narrow chest. Early diagnosis and understanding of this genetic disorder are crucial for managing the symptoms and improving […]
Symptoms and Testing information for PCDH11X Gene Dyslexia Genetic Test
Symptoms of PCDH11X Gene Dyslexia Genetic Test Dyslexia is a common learning difficulty that primarily affects the skills involved in accurate and fluent word reading and spelling. Characterized by difficulties with phonological processing, it can also impact memory, speed of processing, and the language skills necessary for effective reading and writing. In recent years, research […]
Symptoms and Testing information for PDE10A Gene Dyskinesia Limb and Orofacial Infantile-Onset Genetic Test
Symptoms of PDE10A Gene Dyskinesia Limb and Orofacial Infantile-Onset The PDE10A gene plays a critical role in the development and function of the brain, impacting various neurological pathways. Mutations in the PDE10A gene can lead to a rare, yet significant, disorder characterized by dyskinesia of the limbs and orofacial region with an onset in infancy. […]
Symptoms and Testing information for ADCY5 Gene Dyskinesia Familial with Facial Myokymia Genetic Test
Understanding the complexities of genetic disorders is a significant step towards managing and potentially treating them. Among these genetic conditions, ADCY5 gene dyskinesia familial with facial myokymia is one that has garnered attention due to its unique manifestations and the challenges it poses for those affected. DNA Labs UAE is at the forefront of providing […]
Symptoms and Testing information for FRRS1L Gene Dysautonomia FRRS1L-Related Genetic Test
Symptoms of FRRS1L Gene Dysautonomia Dysautonomia associated with the FRRS1L gene presents a complex and multifaceted condition that affects the autonomic nervous system, which controls the involuntary functions of the body, including heart rate, blood pressure, and digestion. This condition can lead to a wide range of symptoms, significantly impacting the quality of life of […]
Symptoms and Testing information for SCN9A Gene Dravet Syndrome Modifier of Genetic Test
Dravet Syndrome is a severe form of epilepsy that begins in infancy. It is characterized by frequent, prolonged seizures often triggered by high temperatures or fever. However, the discovery of the role of the SCN9A gene as a modifier in Dravet Syndrome has opened new avenues for understanding and managing this condition. At DNA Labs […]
Symptoms and Testing information for SCN2A Gene Dravet Syndrome Genetic Test
Understanding the complexities of genetic disorders is crucial for early diagnosis and management. Among these, Dravet Syndrome stands out due to its severe implications on those affected. This condition, primarily caused by mutations in the SCN2A gene, leads to a spectrum of symptoms that can significantly impact the quality of life. At DNA Labs UAE, […]