Cranioectodermal dysplasia, also known as Sensenbrenner syndrome, is a rare genetic disorder that affects multiple parts of the body, including bones, teeth, hair, nails, and kidneys. Type 4 of this condition, specifically associated with mutations in the WDR19 gene, presents unique challenges and symptoms for those affected. Understanding these symptoms is crucial for early diagnosis […]
At DNA Labs UAE, we are committed to providing advanced genetic testing services to help individuals and families understand their genetic makeup and potential health risks. One of the specialized tests we offer is the LONP1 Gene CODAS Syndrome Genetic Test. CODAS Syndrome is a rare genetic disorder that can affect multiple parts of the […]
Coffin-Siris Syndrome (CSS) is a rare genetic disorder that affects multiple organs and systems of the body. It is characterized by developmental delays, intellectual disability, distinctive facial features, and abnormalities of the fifth digits. The syndrome can be caused by mutations in several genes, one of which is the SMARCE1 gene. Understanding the symptoms associated […]
— Cold-Induced Sweating Syndrome (CISS) is a rare genetic disorder primarily characterized by the onset of sweating in cold environments and during infancy. This condition is caused by mutations in the CRLF1 gene. Understanding the symptoms and genetic underpinnings of this disorder is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive […]
The CLCF1 gene plays a crucial role in the human body, influencing various biological processes. A mutation in this gene can lead to Cold-Induced Sweating Syndrome Type 2 (CISS2), a rare genetic disorder. This condition is characterized by a series of symptoms that significantly impact the quality of life of those affected. Understanding these symptoms […]
Understanding PRKD1 Gene Congenital Heart Defects and Ectodermal Dysplasia The PRKD1 gene plays a pivotal role in the normal development of various tissues in the body, including the heart and ectodermal tissues such as skin, hair, nails, and teeth. Mutations in the PRKD1 gene can lead to congenital heart defects and ectodermal dysplasia, conditions that […]
Symptoms of FOXH1 Gene Congenital Heart Disease Congenital heart disease (CHD) refers to a range of birth defects that affect the normal workings of the heart. The FOXH1 gene has been identified as one of the genetic factors contributing to the development of congenital heart disease, including the transposition of the great arteries (TGA). TGA […]
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals and families understand their genetic health. One of the critical tests we offer is for the CLMP gene, associated with Congenital Short-Bowel Syndrome (CSBS). This condition is rare but serious, and early detection through genetic testing can be crucial […]
In the realm of genetic testing, advancements in technology have paved the way for identifying and understanding complex genetic disorders. One such condition that has garnered attention due to its rare and intricate nature is ARX Gene Corpus Callosum Agenesis with Abnormal Genitalia. This genetic disorder is characterized by a range of symptoms that can […]
The LAMC3 gene plays a crucial role in the development and functioning of the human brain. Mutations in this gene can lead to cortical malformations in the occipital region of the brain, a condition that can significantly impact an individual’s neurological and physical health. Recognizing the symptoms associated with LAMC3 gene cortical malformations is essential […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
