Symptoms of IGF1 Gene Growth Retardation with Deafness and Mental Retardation Due to IGF1 Deficiency The IGF1 gene plays a crucial role in human growth and development. Insulin-like Growth Factor 1 (IGF1) is a hormone similar in molecular structure to insulin. It plays an important role in childhood growth and continues to have anabolic effects […]
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 […]
In the complex world of genetics, understanding the role and impact of specific genes on human health is a crucial aspect of medical science. Among these, the HMG20B gene plays a significant role in various biological processes, including neural development. Dysmorphism in the HMG20B gene can lead to a range of health issues, making it […]
Understanding the complexities of genetic disorders is crucial for early diagnosis and treatment. Among these, TP63 Gene Ectodactyly Ectodermal Dysplasia and Cleft Lip/Palate Syndrome Type 3 (EEC Syndrome Type 3) stands out due to its distinctive symptoms and the critical need for accurate diagnosis. DNA Labs UAE is at the forefront of providing comprehensive genetic […]
Ellis-van Creveld syndrome (EVC) is a rare genetic disorder that affects bone growth, leading to skeletal dysplasia among other symptoms. Understanding the signs and symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for EVC, providing a vital tool for families seeking answers. Symptoms of […]
Ellis-van Creveld syndrome (EvC) is a rare genetic disorder that affects bone growth among other physical manifestations. This condition, inherited in an autosomal recessive manner, primarily involves the shortening of the forearms and lower legs (a condition known as mesomelic dwarfism), polydactyly (extra fingers or toes), and abnormalities in the fingernails and teeth. The EVC2 […]
Understanding the symptoms and genetic underpinnings of complex medical conditions is crucial for effective diagnosis and treatment. One such condition, Epiphyseal Dysplasia Multiple with Myopia and Deafness, is linked to mutations in the COL2A1 gene. DNA Labs UAE offers a comprehensive genetic test for this condition, which is essential for individuals experiencing symptoms or with […]
Faciogenital dysplasia, also known as Aarskog-Scott syndrome, is a rare genetic disorder that primarily affects the development of the face, hands, and genitals. It is caused by mutations in the FGD1 gene. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for the […]
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.
