In the realm of genetic testing and diagnostics, the BCS1L gene GRACILE syndrome genetic test stands out as a pivotal assessment for identifying a rare but serious genetic disorder. GRACILE syndrome, an acronym for Growth Retardation, Aminoaciduria, Cholestasis, Iron overload, Lactic acidosis, and Early death, is caused by mutations in the BCS1L gene. This article […]
Symptoms of DHCR24 Gene Desmosterolosis Genetic Test Desmosterolosis, a rare genetic disorder, is caused by mutations in the DHCR24 gene. This condition affects cholesterol biosynthesis, leading to a variety of clinical manifestations. Recognizing the symptoms early is crucial for managing the condition effectively. DNA Labs UAE offers a comprehensive genetic test for DHCR24 gene mutations […]
Fetal Akinesia Deformation Sequence (FADS) is a rare genetic disorder that presents a significant challenge for affected families. This condition, characterized by decreased fetal movement (fetal akinesia), can lead to a range of developmental issues including joint deformities, facial anomalies, lung growth problems, and in severe cases, fetal death. The RAPSN gene plays a crucial […]
Symptoms of RPS28 Gene Diamond Blackfan Anemia Type 15 with Mandibulofacial Dysostosis Genetic Test Diamond Blackfan Anemia (DBA) is a rare genetic blood disorder characterized by the failure of the bone marrow to produce enough red blood cells. This condition can lead to severe anemia and other health issues. Type 15 of this disorder, specifically […]
Fibrochondrogenesis type 1 is a rare genetic disorder that affects the development of the bones and cartilage, leading to significant skeletal abnormalities. This condition is caused by mutations in the COL11A1 gene, which plays a critical role in the production of type XI collagen, a crucial component of the cartilage matrix. Understanding the symptoms of […]
Diamond-Blackfan Anemia (DBA) is a rare inherited bone marrow failure disorder, characterized by an inability of the bone marrow to produce sufficient red blood cells. This leads to anemia and various other complications. A particular subtype of this disorder, known as Diamond-Blackfan Anemia Type 14 with Mandibulofacial Dysostosis, is caused by mutations in the TSR2 […]
Symptoms of TBX1 Gene DiGeorge Syndrome Genetic Test DiGeorge Syndrome, also known as 22q11.2 deletion syndrome, is a disorder caused by a defect in chromosome 22, which affects the development of several body systems. This condition can lead to a range of health issues and developmental delays. The TBX1 gene plays a crucial role in […]
Donnai-Barrow Syndrome (DBS) is a rare genetic disorder that affects multiple systems in the body. It is characterized by distinctive facial features, hearing loss, vision problems, and developmental delays. This condition is caused by mutations in the LRP2 gene, which plays a crucial role in the development of various organs and tissues. Recognizing the symptoms […]
Symptoms of TBC1D24 Gene DOOR Syndrome Genetic Test DOOR syndrome, an acronym for Deafness, Onychodystrophy, Osteodystrophy, and mental Retardation, is a rare genetic disorder caused by mutations in the TBC1D24 gene. This complex condition presents a wide range of symptoms, impacting numerous bodily systems. Recognizing these symptoms early can be crucial for managing the condition […]
Understanding the intricacies of genetic conditions is crucial for early diagnosis and management. Among these conditions, Duane Retraction Syndrome (DRS) stands out due to its unique manifestations and genetic underpinnings. Specifically, mutations in the SALL4 gene have been linked to this condition, making genetic testing a valuable tool for diagnosis. At DNA Labs UAE, we […]
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.
