Symptoms and Testing information for FGFR1 Gene Trigonocephaly Type 1 Genetic Test

Symptoms and Testing information for FGFR1 Gene Trigonocephaly Type 1 Genetic Test

In the realm of genetic diagnostics, the advancements have been nothing short of revolutionary. One such breakthrough has been in the identification and understanding of specific genetic conditions, such as those caused by mutations in the FGFR1 gene, leading to Trigonocephaly Type 1. DNA Labs UAE stands at the forefront of these advancements, offering comprehensive […]

Symptoms and Testing information for C12orf57 Gene Temtamy Syndrome Genetic Test

Symptoms and Testing information for C12orf57 Gene Temtamy Syndrome Genetic Test

Understanding Temtamy Syndrome: A Genetic Overview Temtamy syndrome, a rare genetic disorder, has garnered significant attention within the medical community due to its unique set of symptoms and genetic origins. At DNA Labs UAE, we specialize in providing comprehensive genetic testing services, including the C12orf57 Gene Temtamy Syndrome Genetic Test, to help individuals and families […]

Symptoms and Testing information for WNT10B Gene Split-Handfoot Malformation Type 6 Genetic Test

Symptoms and Testing information for WNT10B Gene Split-Handfoot Malformation Type 6 Genetic Test

In the realm of genetic testing and diagnosis, advancements have been monumental, enabling us to understand the intricacies of the human genome like never before. Among these advancements, DNA Labs UAE stands at the forefront, offering a comprehensive range of genetic tests designed to detect various conditions, including the rare Split-Hand/Foot Malformation Type 6. This […]

Symptoms and Testing information for WNT3 Gene Tetraamelia Autosomal Recessive Genetic Test

Symptoms and Testing information for WNT3 Gene Tetraamelia Autosomal Recessive Genetic Test

DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide insights into your genetic makeup and potential health risks. Among the advanced tests provided is the WNT3 Gene Tetra-Amelia Autosomal Recessive Genetic Test. This particular test is vital for individuals with a family history of tetra-amelia […]

Symptoms and Testing information for NKX3-2 Gene Spondylo-Megaepiphyseal-Metaphyseal Dysplasia Genetic Test

Symptoms and Testing information for NKX3-2 Gene Spondylo-Megaepiphyseal-Metaphyseal Dysplasia Genetic Test

Understanding the complexities of genetic disorders is a challenge that medical science continues to face with determination and innovation. Among these disorders, Spondylo-Megaepiphyseal-Metaphyseal Dysplasia (SMMD), caused by mutations in the NKX3-2 gene, presents a unique set of symptoms and challenges for individuals affected by it. At DNA Labs UAE, we offer a comprehensive genetic test […]

Symptoms and Testing information for CUL7 Gene Three M Syndrome Type 1 Genetic Test

Symptoms and Testing information for CUL7 Gene Three M Syndrome Type 1 Genetic Test

DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide patients and healthcare providers with critical information about genetic conditions. Among these, the CUL7 Gene Three M Syndrome Type 1 Genetic Test is a pivotal tool in diagnosing a rare genetic disorder that affects […]

Symptoms and Testing information for TBX6 Gene Spondylocostal Dysostosis Type 5 Genetic Test

Symptoms and Testing information for TBX6 Gene Spondylocostal Dysostosis Type 5 Genetic Test

Spondylocostal dysostosis is a group of rare inherited disorders characterized by abnormalities in the development of the vertebrae and ribs. Among these, Type 5, associated with mutations in the TBX6 gene, is a condition that has garnered significant attention within the medical and research communities. DNA Labs UAE is at the forefront of providing diagnostic […]

Symptoms and Testing information for OBSL1 Gene Three M Syndrome Type 2 Genetic Test

Symptoms and Testing information for OBSL1 Gene Three M Syndrome Type 2 Genetic Test

Symptoms of OBSL1 Gene Three M Syndrome Type 2 Genetic Test Three M Syndrome is a rare genetic disorder that is characterized by growth retardation, skeletal abnormalities, and distinctive facial features. Type 2 of this syndrome, specifically, is caused by mutations in the OBSL1 gene. Understanding the symptoms associated with this condition is crucial for […]

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