Blogs

Wilson-Turner syndrome is a rare genetic disorder that primarily affects males. It is characterized by intellectual disability, obesity, gynecomastia (enlarged breasts in males), and hypogonadism (decreased function of the gonads). This condition is caused by mutations in the LAS1L gene, which plays a crucial role in the normal development and function of various systems in […]

Understanding the genetic underpinnings of various conditions is crucial for accurate diagnosis and effective management. Among these, the ZC4H2 gene plays a significant role in the development of Wieacker-Wolff Syndrome, a rare X-linked recessive disorder. DNA Labs UAE offers a comprehensive genetic test for this condition, priced at 4400 AED, aimed at identifying mutations in […]

DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide insights into various genetic conditions. Among these, the WDR27 gene-related brain disorders genetic test stands out for its importance in diagnosing conditions associated with mutations in the WDR27 gene. This article delves into the symptoms associated […]

Warburg Micro Syndrome is a rare genetic disorder that significantly impacts the development and function of various parts of the body. This condition is characterized by a wide range of symptoms, primarily affecting the eyes, brain, and reproductive organs. One of the genes associated with this syndrome is RAB3GAP1, and mutations in this gene lead […]

Walker-Warburg Syndrome (WWS) and Muscle-Eye-Brain Disease (MEB) are severe forms of congenital muscular dystrophies associated with brain and eye abnormalities. These conditions are linked to mutations in several genes, including the FKRP gene (Fukutin-Related Protein). Understanding the symptoms and genetic testing options for these diseases is crucial for early diagnosis and management. DNA Labs UAE […]

Symptoms of FKTN Gene Walker-Warburg Syndrome Genetic Test Walker-Warburg Syndrome (WWS) is a severe form of congenital muscular dystrophy associated with brain and eye abnormalities. This condition, primarily affecting the development of the muscle, brain, and eyes, is caused by genetic mutations in several genes, including the FKTN gene. Understanding the symptoms of Walker-Warburg Syndrome […]

Walker-Warburg Syndrome (WWS) is a severe form of congenital muscular dystrophy associated with brain and eye abnormalities. This rare genetic disorder, affecting approximately 1 in every 100,000 live births, is characterized by muscle weakness, developmental delays, and structural brain defects. Understanding the symptoms of WWS is crucial for early diagnosis and intervention. DNA Labs UAE […]

Waardenburg Syndrome and Hirschsprung Disease are two genetic disorders that can significantly impact an individual’s quality of life. Both conditions can arise from mutations in the EDNRB gene, and understanding these mutations is crucial for accurate diagnosis and management. DNA Labs UAE offers a comprehensive genetic test designed to identify mutations in the EDNRB gene, […]

Waardenburg Syndrome (WS) is a rare genetic disorder that affects the color of the skin, hair, and eyes, and can cause hearing loss. Type 2D of this syndrome, specifically, is linked to mutations in the SNAI2 gene. DNA Labs UAE offers a comprehensive genetic test for those who suspect they might carry this specific mutation, […]

In the realm of genetic testing, advancements have allowed us to identify and manage various inherited conditions with greater precision and understanding than ever before. Among these conditions is Vitamin E deficiency due to mutations in the TTPA gene, a rare, autosomal recessive disorder that can lead to significant neurological problems if not diagnosed and […]