Symptoms and Testing information for ERCC4 Gene XFE Progeroid Syndrome Genetic Test

Symptoms and Testing information for ERCC4 Gene XFE Progeroid Syndrome Genetic Test

— Understanding the symptoms of ERCC4 Gene XFE Progeroid Syndrome is crucial for early detection and management of this rare genetic condition. At DNA Labs UAE, we are committed to providing comprehensive genetic testing services, including tests for the ERCC4 Gene XFE Progeroid Syndrome. This genetic test is priced at 4400 AED and is a […]

Symptoms and Testing information for ZIC5 Gene ZIC5 Related Brain Disorders Genetic Test

Symptoms and Testing information for ZIC5 Gene ZIC5 Related Brain Disorders Genetic Test

DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide range of services designed to provide valuable insights into various genetic disorders. Among the numerous tests available, the ZIC5 Gene ZIC5 Related Brain Disorders Genetic Test stands out due to its significance in diagnosing brain disorders linked to the ZIC5 […]

Symptoms and Testing information for EPG5 Gene Vici Syndrome Genetic Test

Symptoms and Testing information for EPG5 Gene Vici Syndrome Genetic Test

Vici syndrome is a rare genetic disorder characterized by a spectrum of clinical manifestations, primarily affecting the brain, immune system, heart, skin, and eyes. It is caused by mutations in the EPG5 gene, which plays a crucial role in the autophagic process, essential for the degradation and recycling of cellular components. Recognizing the symptoms early […]

Symptoms and Testing information for ACTG2 Gene Visceral Myopathy Genetic Test

Symptoms and Testing information for ACTG2 Gene Visceral Myopathy Genetic Test

Visceral myopathy is a rare genetic disorder that affects the smooth muscles of the gastrointestinal tract, leading to a wide range of digestive problems. One of the genes associated with this condition is the ACTG2 gene. Mutations in this gene can lead to various symptoms that can significantly impact an individual’s quality of life. Understanding […]

Symptoms and Testing information for DDX11 Gene Warsaw Breakage Syndrome Genetic Test

Symptoms and Testing information for DDX11 Gene Warsaw Breakage Syndrome Genetic Test

Symptoms of DDX11 Gene Warsaw Breakage Syndrome Genetic Test Warsaw Breakage Syndrome, attributed to mutations in the DDX11 gene, is a rare genetic disorder. Recognizing its symptoms is critical for early diagnosis and management. DDX11 gene mutations can lead to a spectrum of clinical manifestations, primarily characterized by growth retardation, microcephaly (small head size), and […]

Symptoms and Testing information for EZH2 Gene Weaver Syndrome Genetic Test

Symptoms and Testing information for EZH2 Gene Weaver Syndrome Genetic Test

DNA Labs UAE is at the forefront of genetic testing and diagnosis, offering a wide range of services to help individuals understand their genetic makeup and potential health risks. One of the critical tests offered by DNA Labs UAE is the EZH2 Gene Weaver Syndrome Genetic Test. This test is crucial for diagnosing Weaver Syndrome, […]

Symptoms and Testing information for ARNT2 Gene Webb-Dattani Syndrome Genetic Test

Symptoms and Testing information for ARNT2 Gene Webb-Dattani Syndrome Genetic Test

In the realm of genetic diagnostics, the advancements have been profound, particularly in identifying and managing rare genetic disorders. One such condition, Webb-Dattani Syndrome, is associated with mutations in the ARNT2 gene. DNA Labs UAE stands at the forefront of these advancements, offering a comprehensive genetic test specifically designed to detect mutations in the ARNT2 […]

Symptoms and Testing information for LTBP2 Gene Weill-Marchesani Syndrome Type 3 Genetic Test

Symptoms and Testing information for LTBP2 Gene Weill-Marchesani Syndrome Type 3 Genetic Test

Understanding the intricate world of genetics has paved the way for significant advancements in the diagnosis and management of various hereditary conditions. Among these, Weill-Marchesani Syndrome (WMS) stands out due to its rarity and the complex spectrum of symptoms it presents. Specifically, Type 3 WMS, linked to mutations in the LTBP2 gene, poses unique challenges […]

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