Understanding the complexities of genetic conditions is crucial for early diagnosis and management. Among these conditions, Short-Rib Thoracic Dysplasia Type 4 with or without Polydactyly, linked to mutations in the TTC21B gene, stands out due to its distinctive symptoms and implications. DNA Labs UAE offers a comprehensive genetic test for this condition, providing families and […]
Understanding Short-Rib Thoracic Dysplasia Type 5 Short-Rib Thoracic Dysplasia Type 5, also known as Jeune Syndrome, is a rare genetic disorder characterized by a narrow thorax, short ribs, short limbs, and, in some cases, polydactyly. This condition falls under the category of ciliopathies, which are disorders associated with the dysfunction of cilia, microscopic hair-like structures […]
Symptoms of NEK1 Gene Short-Rib Thoracic Dysplasia Type 6 with or Without Polydactyly Short-Rib Thoracic Dysplasia Type 6 (SRTD6), associated with or without polydactyly, is a rare genetic disorder that is part of a group of diseases known as ciliopathies. The NEK1 gene plays a critical role in the development and function of cilia, which […]
Understanding the genetic underpinnings of rare diseases is crucial for early diagnosis, management, and treatment. One such condition is Short-Rib Thoracic Dysplasia Type 7 with or Without Polydactyly, caused by mutations in the WDR35 gene. This article delves into the symptoms associated with this genetic disorder and introduces a comprehensive genetic test offered by DNA […]
Short-Rib Thoracic Dysplasia (SRTD) encompasses a group of rare genetic disorders characterized by abnormalities in the development of the bones of the rib cage and other regions of the body. Type 8 of this disorder, specifically linked to mutations in the WDR60 gene, can present with or without polydactyly – the presence of extra fingers […]
Shprintzen-Goldberg Syndrome (SGS) is a rare genetic disorder that affects multiple organ systems. It is characterized by craniosynostosis (premature fusion of skull bones), distinctive facial features, skeletal abnormalities, and intellectual disability. The syndrome is caused by mutations in the SKI gene, which plays a crucial role in regulating cellular growth and development. Understanding the symptoms […]
Understanding Chr. 11p15 Gene Silver-Russell Syndrome Silver-Russell Syndrome (SRS) is a rare congenital disorder, characterized by growth restriction before birth, leading to low birth weight and subsequent growth problems after birth. This condition is also associated with distinctive facial features, asymmetry of body parts, and other developmental anomalies. A crucial factor in diagnosing this syndrome […]
In the realm of genetic diagnostics and family health, understanding the implications of certain genetic conditions is paramount for early intervention and treatment. Among these conditions, Silver-Russell Syndrome (SRS) stands out due to its distinctive features and the unique genetic mechanisms behind its occurrence. At DNA Labs UAE, we are committed to providing comprehensive genetic […]
In the realm of genetic diagnostics, understanding the intricate details of our DNA can unlock answers to many health-related questions, including the predisposition to certain conditions. Among these, skeletal abnormalities associated with the CBFB gene represent a critical area of study. At DNA Labs UAE, we offer a comprehensive genetic test specifically designed to detect […]
Symptoms of ZBTB16 Gene Skeletal Defects, Genital Hypoplasia, and Mental Retardation Understanding the complex nature of genetic disorders is crucial for early diagnosis and treatment. One such genetic condition involves mutations in the ZBTB16 gene, which can lead to a constellation of symptoms including skeletal defects, genital hypoplasia, and mental retardation. Recognizing these symptoms early […]
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.
