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Symptoms and Testing information for ATP1A3 Gene DYT12 Genetic Test

Symptoms and Testing information for ATP1A3 Gene DYT12 Genetic Test

Understanding the symptoms of the ATP1A3 gene mutation, associated with DYT12 genetic disorder, is crucial for early diagnosis and effective management of the condition. DNA Labs UAE offers a comprehensive genetic test for this mutation, providing valuable insights into this rare but impactful condition. The test, priced at 4400 AED, is a critical tool for […]

Symptoms and Testing information for DRD2 Gene DYT11 DRD2 Related Genetic Test

Symptoms and Testing information for DRD2 Gene DYT11 DRD2 Related Genetic Test

In the realm of genetic testing, understanding the nuances of our DNA can provide invaluable insights into our health, predispositions, and potential medical conditions. One particular area of interest is the DRD2 gene, also associated with the DYT11 movement disorder. DNA Labs UAE is at the forefront of offering comprehensive genetic testing services, including the […]

Symptoms and Testing information for SGCE Gene DYT11 Genetic Test

Symptoms and Testing information for SGCE Gene DYT11 Genetic Test

— The SGCE gene, also known as the epsilon-sarcoglycan gene, plays a crucial role in the normal functioning of the brain, particularly in the movement control regions. Mutations in this gene are associated with a condition known as Myoclonus-Dystonia (MD), which is classified under the broader category of dystonia, DYT11. Understanding the symptoms of SGCE […]

Symptoms and Testing information for PRRT2 Gene DYT10 Genetic Test

Symptoms and Testing information for PRRT2 Gene DYT10 Genetic Test

Understanding the Symptoms of PRRT2 Gene DYT10 Genetic Test The PRRT2 gene mutation is associated with a range of neurological conditions, most notably DYT10, also known as paroxysmal kinesigenic dyskinesia (PKD). This condition is characterized by sudden, brief, involuntary movements or spasms that are triggered by sudden motion. Understanding the symptoms associated with this genetic […]

Symptoms and Testing information for TOR1A Gene DYT1 Genetic Test

Symptoms and Testing information for TOR1A Gene DYT1 Genetic Test

In the realm of medical genetics, understanding the intricacies of our DNA can provide crucial insights into numerous conditions that affect human health. One such condition is associated with mutations in the TOR1A gene, which is linked to a specific form of dystonia known as DYT1 dystonia. This disorder is characterized by involuntary muscle contractions […]

Symptoms and Testing information for TIMM8A Gene Dystonia-Deafness Syndrome Genetic Test

Symptoms and Testing information for TIMM8A Gene Dystonia-Deafness Syndrome Genetic Test

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 […]

Symptoms and Testing information for SPR Gene Dystonia DOPA-Responsive Autosomal Recessive Genetic Test

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

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

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 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 […]

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