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Symptoms and Testing information for FXN Gene Friedreich Ataxia Genetic Test
Friedreich ataxia (FRDA) is a rare, inherited disease that causes progressive damage to the nervous system. It manifests in symptoms ranging from gait disturbance and speech problems to heart disease. The condition is named after the physician Nicholaus Friedreich, who first described the syndrome in the 1860s. It’s caused by a defect in the FXNSymptoms and Testing information for ROBO3 Gene Gaze Palsy Horizontal with Progressive Scoliosis Genetic Test
Understanding the complexities of genetic conditions is pivotal in modern healthcare. Among these conditions, a particularly intriguing one is associated with the ROBO3 gene, which can lead to gaze palsy horizontal with progressive scoliosis. This condition is rare and often requires specialized genetic testing for accurate diagnosis and management. DNA Labs UAE stands at theSymptoms and Testing information for RYR1 Gene Central Core Disease Genetic Test
Central Core Disease (CCD) is a rare genetic condition that affects the muscles, leading to muscle weakness, skeletal abnormalities, and in some cases, susceptibility to malignant hyperthermia (MH), a severe reaction to certain anesthesia drugs. The condition is named after the characteristic appearance of the muscle fibers observed under a microscope, showing areas of disorganizationSymptoms and Testing information for APOE Gene Alzheimer disease type 2 Genetic Test
Understanding the APOE Gene and Its Role in Alzheimer’s Disease Type 2 The APOE gene is one of the most extensively studied genes in connection to Alzheimer’s disease. This gene comes in several variants, with APOE ε2, ε3, and ε4 being the most common. The presence of the APOE ε4 allele is known to increaseSymptoms and Testing information for ATRX Gene Alpha-thalassemiamental retardation syndrome Genetic Test
The ATRX Gene Alpha-thalassemia/mental retardation syndrome (ATR-X) is a rare and complex genetic condition that affects various aspects of physical and intellectual development. This condition, primarily found in males, is characterized by a combination of alpha-thalassemia, a blood disorder that reduces the production of hemoglobin, and mental retardation, along with a variety of other possibleSymptoms and Testing information for MAF Gene Cataract Pulverulent or Cerulean with or without Microcornea Genetic Test
Understanding the complexities of genetic disorders is essential in today’s medical landscape, especially when it comes to conditions that can significantly impact quality of life from a very young age. One such condition involves the mutation of the MAF gene, which has been linked to specific types of cataracts, namely Pulverulent and Cerulean cataracts, withSymptoms and Testing information for CTC1 Gene Coat Plus Syndrome Genetic Test
DNA Labs UAE is at the forefront of genetic testing and analysis, offering a wide array of services designed to provide insights into one’s genetic makeup. Among these services is the CTC1 Gene Coat Plus Syndrome Genetic Test, a comprehensive examination aimed at detecting the presence of mutations in the CTC1 gene, which can indicate
Genealogy Family Tree & Ancestry DNA Test UAE
Unlock your family's story and take control of your health with our Genealogy DNA Test. Gain insights into your ancestry and discover connections you never knew existed.
- Price & Value: 1500 AED (All Inclusive)
- Convenience: Premium Home Sample Collection (Across UAE - 100 AED)
- Turnaround: Get results in 4-6 weeks
- Standard: ISO 9001:2015 Certified Accuracy
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