The BCS1L Gene GRACILE Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the BCS1L gene, which are responsible for GRACILE Syndrome. GRACILE Syndrome is a rare genetic disorder characterized by growth retardation, aminoaciduria, cholestasis, iron overload, lactic acidosis, and early death. This condition is inherited in an autosomal recessive manner, meaning that both copies of the gene in each cell have mutations.

The test is particularly crucial for families with a history of the syndrome or individuals showing symptoms related to the condition. Early detection through this genetic test can lead to a better understanding of the disease, allowing for more targeted management and care strategies for affected individuals. The test involves analyzing the patient’s DNA to look for specific mutations in the BCS1L gene, which plays a crucial role in the normal function of mitochondria.

DNA Labs UAE offers this comprehensive genetic testing service for a cost of 4400 AED. The test is conducted in a state-of-the-art laboratory setting by experienced geneticists and technicians, ensuring high accuracy and reliability of the results. Upon completion, a detailed report is provided, offering insights into the presence of any genetic mutations associated with GRACILE Syndrome and guidance for further steps. This test is an invaluable tool for affected families, providing them with critical information for making informed health and lifestyle decisions.