In the realm of genetic diagnostics, understanding the nuances of genetic mutations and their implications on health is paramount. One such critical area of focus is the KIT gene and its association with Gastrointestinal Stromal Tumors (GISTs). At DNA Labs UAE, we specialize in providing comprehensive genetic testing services, including the KIT Gene Gastrointestinal Stromal […]
Oncology Diseases
Symptoms and Testing information for CCND1 Gene Colorectal Cancer Hereditary Susceptibility to Genetic Test
Colorectal cancer is a major health concern worldwide, with a significant number of cases attributed to hereditary factors. Understanding the genetic predisposition to this disease is crucial for early detection and prevention. One of the key genes associated with an increased risk of developing colorectal cancer is the CCND1 gene. This article delves into the […]
Symptoms and Testing information for XRCC3 Gene Breast Cancer Susceptibility to Genetic Test
Understanding the genetic predispositions to various diseases has been a cornerstone in modern medicine, enabling early detection and proactive management of numerous conditions. Among these, breast cancer remains one of the most significant concerns for women worldwide. The discovery of the XRCC3 gene’s role in breast cancer susceptibility has been a breakthrough, offering hope and […]
Symptoms and Testing information for RAD51C Gene Breast-Ovarian Cancer Genetic Test
Symptoms of RAD51C Gene Breast-Ovarian Cancer Genetic Test Cancer, a word that strikes fear into the hearts of many, has various forms and manifestations. Among them, breast and ovarian cancers are significant concerns for women worldwide. Understanding the genetic predispositions to these cancers can be a powerful tool in combating them. One such genetic marker […]
Symptoms and Testing information for RAD51D Gene Breast-Ovarian Cancer Familial Susceptibility to Type 4 Genetic Test
In the realm of genetic testing and personalized medicine, understanding one’s genetic predisposition to certain cancers is a significant step toward preventative health care. Among the myriad genetic tests available, the RAD51D gene breast-ovarian cancer familial susceptibility to type 4 genetic test stands out for its importance in assessing the risk of developing breast and […]
Symptoms and Testing information for CALR Gene CALR Selective Sequencing of Exon 9 Genetic Test
The CALR gene, known scientifically as Calreticulin, plays a significant role in the human body, impacting various physiological processes, including calcium homeostasis and the proper functioning of the immune system. Mutations in this gene have been closely associated with certain types of blood disorders, particularly Myeloproliferative Neoplasms (MPNs). MPNs are a group of disorders characterized […]
Symptoms and Testing information for SDHD Gene Carcinoid Tumors Intestinal Genetic Test
In the realm of genetic diagnostics and personalized medicine, understanding the intricate relationship between our genes and health conditions is paramount. Among the myriad of genetic disorders, carcinoid tumors associated with the SDHD gene represent a significant area of concern due to their potential impact on the intestinal tract. DNA Labs UAE, a leading genetic […]
Symptoms and Testing information for PRKAR1A Gene Carney Complex Type 1 Genetic Test
The PRKAR1A gene plays a pivotal role in the normal functioning of the body’s cells, influencing how they grow, divide, and communicate with one another. Mutations in this gene are associated with Carney Complex Type 1, a rare genetic disorder that affects multiple systems in the body and predisposes individuals to various benign and malignant […]
Symptoms and Testing information for CDC20 Gene Cell Cycle Disorder CDC20 Related Genetic Test
Understanding the CDC20 Gene Cell Cycle Disorder and the Importance of CDC20 Related Genetic Testing The CDC20 gene plays a critical role in the cell cycle, specifically in the activation of the anaphase-promoting complex/cyclosome (APC/C), which is essential for the transition from metaphase to anaphase during cell division. Mutations or dysregulation in the CDC20 gene […]
Symptoms and Testing information for CDKN1C Gene Beckwith-Wiedemann Syndrome Genetic Test
Beckwith-Wiedemann Syndrome (BWS) is a complex genetic disorder that affects many parts of the body. It is characterized by a wide range of symptoms and features, which can vary significantly from one individual to another. The syndrome is primarily known for causing overgrowth and an increased risk of developing childhood cancer. The CDKN1C gene plays […]