Understanding Bardet-Biedl Syndrome Type 14 Bardet-Biedl Syndrome (BBS) is a complex genetic condition that affects multiple organ systems within the body. Among its various types, Type 14, linked with mutations in the CEP290 gene, is one of the notable subtypes. This condition is characterized by symptoms that can impact an individual’s quality of life significantly. […]
Understanding MKS1 Gene Bardet-Biedl Syndrome Type 13 Bardet-Biedl Syndrome (BBS) is a complex genetic disorder that affects many parts of the body. Among the different types of BBS, Type 13, caused by mutations in the MKS1 gene, is notable for its wide range of symptoms and impacts on health. Recognizing the symptoms early can be […]
Bardet-Biedl Syndrome (BBS) is a complex genetic disorder that affects many parts of the body. Among the numerous genes associated with this condition, mutations in the BBS12 gene lead to Bardet-Biedl Syndrome Type 12. Individuals and families grappling with the symptoms of this condition or with a history of BBS can now turn to DNA […]
In the realm of genetic testing, advancements have paved the way for early detection and management of various genetic disorders. Among these, Bardet-Biedl Syndrome (BBS) represents a complex condition that affects multiple body systems. Type 11 of this syndrome, linked to mutations in the TRIM32 gene, underscores the importance of genetic testing for individuals showing […]
Bardet-Biedl Syndrome (BBS) is a complex genetic disorder affecting multiple body systems. Among the various genes associated with BBS, mutations in the BBS10 gene are responsible for Bardet-Biedl Syndrome Type 10. Recognizing the symptoms associated with this genetic condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for […]
Bardet-Biedl Syndrome (BBS) is a complex genetic condition that affects many parts of the body. Among the various genes associated with this disorder, mutations in the BBS1 gene are the most common cause of Bardet-Biedl Syndrome Type 1. Recognizing the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers […]
Arthrogryposis Renal Dysfunction and Cholestasis (ARC) syndrome is a rare genetic disorder that affects multiple body systems, including the joints, kidneys, and liver. Type 2 of this syndrome, specifically linked to mutations in the VIPAS39 gene, presents a unique set of challenges and symptoms for those affected. At DNA Labs UAE, we offer a comprehensive […]
DNA Labs UAE is a premier genetic testing facility dedicated to providing accurate, comprehensive, and confidential genetic testing services. One of the critical tests offered by DNA Labs UAE is the SHBG Gene Androgen-Binding Protein Deficiency Genetic Test. This test is essential for individuals experiencing symptoms that may indicate a deficiency in the Sex Hormone […]
Androgen Insensitivity Syndrome (AIS) is a condition that affects sexual development before birth and during puberty. It is caused by mutations in the AR gene, which is essential for directing male sexual development. This condition is part of a spectrum, with partial androgen insensitivity syndrome (PAIS) being one of its forms. PAIS can result in […]
Androgen insensitivity syndrome (AIS) is a genetic condition that affects sexual development before birth and during puberty. People with this condition are genetically male, with one X chromosome and one Y chromosome in each cell. However, their bodies are unable to respond properly to male sex hormones (androgens). This can lead to the development of […]
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.
