Dysmorphology Diseases

Symptoms of GLI3 Gene Greig Cephalopolysyndactyly Syndrome Genetic Test Greig cephalopolysyndactyly syndrome (GCPS) is a rare genetic disorder that affects the development of the limbs, head, and face. The condition is primarily caused by mutations in the GLI3 gene, which plays a crucial role in regulating the growth and development of these body parts. Recognizing […]

Understanding the complexities of genetic conditions is essential for early diagnosis and appropriate management. One such rare genetic disorder is characterized by fibular aplasia or hypoplasia, femoral bowing, and poly-, syn-, and oligodactyly, which involves mutations in the WNT7A gene. This condition, while rare, presents a unique set of symptoms that can significantly impact an […]

In the quest to understand the complexities of human genetics and its implications on health, DNA Labs UAE has emerged as a leader, providing comprehensive genetic testing services to help individuals and healthcare professionals make informed decisions. Among its suite of tests, the GHR Gene Growth Hormone Insensitivity Partial Genetic Test stands out for its […]

Symptoms of POLE Gene FILS Syndrome Genetic Test POLE gene FILS syndrome is a rare genetic disorder that has garnered significant attention within the medical community for its complex presentation and the critical need for accurate diagnosis. DNA Labs UAE stands at the forefront of genetic testing, offering a comprehensive solution for families seeking answers. […]

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 […]

FRAS1 gene Fraser Syndrome is a rare genetic disorder that affects development before birth. This condition is characterized by a wide spectrum of abnormalities affecting the skin, eyes, and kidneys. Understanding the symptoms of this syndrome is crucial for early diagnosis and intervention. DNA Labs UAE offers a comprehensive genetic test for the FRAS1 gene […]

Understanding the FTO Gene and Its Implications The FTO gene, associated with fat mass and obesity, has been extensively studied for its role in weight regulation. However, recent research has unveiled its significance in other critical developmental areas, including growth retardation, developmental delay, and facial dysmorphism. These conditions can significantly impact the quality of life […]

Symptoms of FREM2 Gene Fraser Syndrome Genetic Test Fraser syndrome, a rare autosomal recessive disorder, is primarily characterized by cryptophthalmos, syndactyly, and abnormalities in the kidneys, among other clinical manifestations. The FREM2 gene plays a crucial role in the development of these symptoms. Understanding the symptoms is essential for early diagnosis and management of the […]

The HOXA13 gene plays a crucial role in the development of the limbs, gastrointestinal tract, and the urinary system. Mutations in this gene can lead to Guttmacher Syndrome, a rare genetic disorder characterized by a spectrum of abnormalities affecting these systems. Recognizing the symptoms of Guttmacher Syndrome is essential for early diagnosis and management. DNA […]

Symptoms of GRIP1 Gene Fraser Syndrome Genetic Test Fraser syndrome, a rare autosomal recessive genetic disorder, has been a subject of concern for many families. This condition is characterized by cryptophthalmos, syndactyly, abnormalities in the genitalia, and sometimes renal agenesis. Recognizing the symptoms early can significantly impact the management and prognosis of the condition. DNA […]