Dysmorphology Diseases

Carpenter Syndrome, also known as Acrocephalopolysyndactyly Type II, is a rare genetic disorder that affects multiple parts of the body, including the skull, fingers, toes, heart, and obesity. It is a subtype of a broader category of diseases known as ciliopathies, which are disorders associated with defects in the structure or function of cilia, the […]

— Bainbridge-Ropers Syndrome (BRS) is a rare genetic disorder that affects multiple aspects of a patient’s health and development. It is caused by mutations in the ASXL3 gene, which plays a crucial role in the regulation of gene expression. DNA Labs UAE offers a comprehensive genetic test for those who suspect they or their family […]

Understanding the complexities of genetic conditions is crucial for early diagnosis and management. Among these, the mutation of the OCLN gene leading to Band-Like Calcification with Simplified Gyration and Polymicrogyria (BLC-SGP) is a rare but significant disorder that affects the brain’s development. DNA Labs UAE offers a comprehensive genetic test for this condition, providing invaluable […]

At DNA Labs UAE, we understand the complexities and concerns that come with genetic conditions, and we are committed to providing our clients with accurate, comprehensive genetic testing services. One such service we offer is the ACTB Gene Baraitser-Winter Syndrome Type 1 Genetic Test. This detailed examination is crucial for individuals suspecting they might have […]

Baraitser-Winter Syndrome Type 2, a rare genetic disorder, significantly impacts those affected and their families. Understanding this condition and its associated symptoms is crucial for early diagnosis and management. DNA Labs UAE is at the forefront of genetic testing, offering comprehensive services including the ACTG1 Gene Baraitser-Winter Syndrome Type 2 Genetic Test. This detailed examination […]

DNA Labs UAE is at the forefront of genetic testing, providing comprehensive services to diagnose a wide range of genetic conditions. Among these, the PTCH1 Gene Basal Cell Nevus Syndrome Genetic Test stands out for its importance in diagnosing Basal Cell Nevus Syndrome (BCNS), also known as Gorlin Syndrome. This test, priced at 4400 AED, […]

DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of tests tailored to detect a variety of genetic conditions. Among these, the SUFU Gene Basal Cell Nevus Syndrome Genetic Test stands out as a crucial tool for diagnosing a condition that, if left unchecked, could lead to severe […]

Symptoms of SLC20A2 Gene Basal Ganglia Calcification Type 1 Ideopathic Genetic Test The SLC20A2 gene plays a pivotal role in phosphate regulation within the human body, and mutations in this gene can lead to Basal Ganglia Calcification Type 1, also known as Idiopathic Basal Ganglia Calcification (IBGC1) or Fahr’s Disease. This condition is characterized by […]

Understanding the intricate nature of our genetics has always been a cornerstone of medical science. It is through this understanding that we can uncover the mysteries behind various genetic disorders, one of which is the PDGFRB Gene Basal Ganglia Calcification Type 4. This condition, while rare, can have a significant impact on those affected. DNA […]

Understanding the symptoms of PDGFB Gene Basal Ganglia Calcification Type 5 Idiopathic and the significance of genetic testing for this condition is crucial for early diagnosis and management. PDGFB Gene Basal Ganglia Calcification Type 5, also known as Idiopathic Basal Ganglia Calcification (IBGC) Type 5, is a genetic disorder characterized by the abnormal accumulation of […]