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 […]
Dysmorphology Diseases
Symptoms and Testing information for POLR1C Gene Treacher Collins Syndrome Type 3 Genetic Test
Treacher Collins Syndrome (TCS) is a genetic disorder characterized by craniofacial deformities, arising from mutations in specific genes. Type 3 TCS, in particular, is associated with mutations in the POLR1C gene. Understanding the symptoms and the importance of genetic testing for this condition can significantly impact the lives of affected individuals and their families. DNA […]
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 WNT7A Gene Ulna and Fibula Absence of with Severe Limb Deficiency Genetic Test
Understanding the WNT7A Gene and Its Impact on Limb Development The WNT7A gene plays a crucial role in the development of limbs in the human body. Mutations in this gene can lead to severe limb deficiencies, including the absence of the ulna and fibula, two bones essential for the proper structure and function of the […]
Symptoms and Testing information for TBX3 Gene Ulnar-Mammary Syndrome Genetic Test
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive suite of tests that cater to a wide array of genetic conditions. Among these, the TBX3 Gene Ulnar-Mammary Syndrome Genetic Test stands out for its significance in diagnosing a rare genetic disorder that affects various parts of the body, including […]
Symptoms and Testing information for LRIG2 Gene Urofacial Syndrome Genetic Test
Urofacial Syndrome, also known as Ochoa Syndrome, is a rare genetic disorder that affects the urinary tract and facial expressions. This condition is often underdiagnosed or misdiagnosed due to the variability of its symptoms. The LRIG2 gene has been identified as a significant factor in the development of Urofacial Syndrome. Understanding the symptoms of this […]
Symptoms and Testing information for HPSE2 Gene Urofacial Syndrome Type 1 Genetic Test
Urofacial Syndrome (UFS) or Ochoa Syndrome is a rare genetic disorder characterized by a distinctive facial expression and abnormalities in urinary tract function. The condition, primarily caused by mutations in the HPSE2 gene, leads to what is known as Urofacial Syndrome Type 1. Recognizing the symptoms early and opting for genetic testing can be crucial […]
Symptoms and Testing information for SCARF2 Gene Van den Ende-Gupta Syndrome Genetic Test
Van den Ende-Gupta syndrome (VDEGS) is a rare genetic disorder characterized by a range of physical anomalies and developmental delays. It is caused by mutations in the SCARF2 gene. This condition, although rare, requires precise diagnosis for appropriate management and intervention. In the UAE, DNA Labs UAE offers a comprehensive genetic test for the SCARF2 […]
Symptoms and Testing information for CCDC8 Gene Three M Syndrome Type 3 Genetic Test
Understanding the nuances and implications of genetic disorders is crucial for early diagnosis and appropriate management. One such rare genetic condition is the Three M Syndrome Type 3, caused by mutations in the CCDC8 gene. DNA Labs UAE offers a comprehensive genetic test for this condition, aiming to provide crucial insights for affected individuals and […]
Symptoms and Testing information for IRF6 Gene Van der Woude Syndrome Type 1 Genetic Test
Van der Woude Syndrome Type 1 (VWS1) is a genetic condition that is primarily known for its orofacial manifestations. It is an autosomal dominant disorder, meaning that only one copy of the altered gene is sufficient to cause the disorder. The gene implicated in this condition is the IRF6 gene, which plays a crucial role […]