Are you looking for ? | Page 20 of 25

Symptoms and Testing information for LMNA Gene Cardiomyopathy dilated with hypergonadotropic hypogonadism Genetic Test

DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive array of services aimed at providing insights into various genetic conditions. One of the pivotal tests offered by DNA Labs UAE is for the diagnosis of a specific genetic condition related to the LMNA gene, known as LMNA Gene Cardiomyopathy

Symptoms and Testing information for MYH6 Gene Cardiomyopathy Dilated Type 1EE Genetic Test

Symptoms of MYH6 Gene Cardiomyopathy Dilated Type 1EE Genetic Test Cardiomyopathy is a disease that affects the muscle tissue of the heart, making it harder for the heart to pump blood to the rest of the body. One specific form, Dilated Cardiomyopathy (DCM), involves the enlargement of the heart’s chambers and thinning of its walls,

Symptoms and Testing information for TIMP1 Gene Bicuspid Aortic Valve Genetic Test

Understanding the genetic underpinnings of heart conditions can significantly impact the approach to prevention, diagnosis, and treatment. Among these conditions, the Bicuspid Aortic Valve (BAV) disorder stands out due to its prevalence and potential complications. Recent advancements in genetic testing, particularly concerning the TIMP1 gene, have paved the way for early detection and management strategies.

Symptoms and Testing information for ACTC1 Gene Atrial Septal Defect Type 5 Genetic Test

Understanding the symptoms and genetic underpinnings of Atrial Septal Defect Type 5 (ASD5) is crucial for early diagnosis and treatment. This condition, associated with mutations in the ACTC1 gene, represents a significant concern for individuals and families affected by it. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the

Symptoms and Testing information for PIK3R1 Gene Immunodeficiency Type 36 Genetic Test

In the realm of medical genetics, understanding the intricate dance of DNA and its impact on health has become a cornerstone of modern medicine. One such condition that has come under the spotlight is PIK3R1 Gene Immunodeficiency Type 36. This rare genetic disorder can lead to a host of immune system problems, making it crucial

Symptoms and Testing information for GJB4 Gene Erythrokeratodermia variabilis et progressive Genetic Test

Erythrokeratodermia variabilis et progressive (EKVP) is a rare genetic skin disorder characterized by the presence of both fixed, persistent erythrokeratoderma and transient erythematous patches. This condition is caused by mutations in the GJB4 gene, which encodes a protein known as connexin 30.3, playing a crucial role in the communication between skin cells. Recognizing the symptoms

Symptoms and Testing information for FLG Gene Dermatitis Atopic Type 2 Genetic Test

Symptoms of FLG Gene Dermatitis Atopic Type 2 Genetic Test Atopic dermatitis, commonly known as eczema, is a chronic skin condition that affects millions worldwide. A significant breakthrough in understanding this condition has been the identification of genetic factors contributing to its development. One such genetic factor is mutations in the FLG gene, which codes

Symptoms and Testing information for MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy Genetic Test

Understanding the complexities of genetic disorders is crucial in the realm of modern medicine. Among these, a rare but significant condition to be aware of is Diarrhea Type 2 with Microvillus Atrophy, which is linked to mutations in the MYO5B gene. This condition presents a spectrum of symptoms that can be distressing for the affected

Symptoms and Testing information for AMBN Gene Amelogenesis Imperfecta Type 1F Genetic Test

Amelogenesis Imperfecta (AI) is a genetic condition that affects the development of the enamel, the hard, protective outer layer of the teeth. Type 1F, associated with mutations in the AMBN gene, is a specific subtype of this condition. DNA Labs UAE offers a comprehensive genetic test for this condition, providing invaluable information for affected individuals

Symptoms and Testing information for P2RX2 Gene Progressive Hearing Loss Genetic Test

Symptoms of P2RX2 Gene Progressive Hearing Loss Genetic Test Hearing loss can be a challenging condition that affects individuals of all ages, impacting their quality of life and ability to communicate effectively. Among the various causes of hearing impairment, genetic factors play a significant role. The P2RX2 gene is one such genetic component that has

Browse

Want to chat?

Social

Search Results for: accessibility