Symptoms of Nicotine and Cotinine Urine Test Nicotine, a potent chemical found in cigarettes, cigars, and other tobacco products, swiftly makes its way into the bloodstream upon inhalation. Its primary metabolite, cotinine, is used as a biomarker to measure exposure to tobacco smoke. The Nicotine and Cotinine Urine Test, offered by DNA Labs UAE, is […]
Genetic Diseases
Symptoms and Testing information for Prader-Willi Syndrome Mutation Detection Methylation Specific PCR Test
Prader-Willi Syndrome (PWS) is a rare genetic disorder that affects many parts of the body. It is characterized by a variety of symptoms and signs which typically manifest from infancy through adulthood. Early diagnosis and intervention are crucial for managing the condition effectively. One of the most reliable methods for diagnosing PWS is through the […]
Symptoms and Testing information for Fragile X FMR1 Mutation Screen Test
Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. It is the most common form of inherited intellectual disability in males and a significant cause of intellectual disability in females. The syndrome is related to the expansion of the CGG triplet repeat within the […]
Symptoms and Testing information for ALL Panel Deletion/Duplication Detection Test
Understanding the Symptoms of ALL Panel Deletion/Duplication Detection Test Acute Lymphoblastic Leukemia (ALL) is a type of cancer that affects the white blood cells, playing a crucial role in the body’s immune system. It progresses rapidly, making early detection and treatment essential for improving the prognosis. One of the advanced diagnostic methods available is the […]
Symptoms and Testing information for AML PCR Panel AMLETO Inv16 PMLRARA Test
Acute Myeloid Leukemia (AML) is a serious and fast-growing form of cancer that affects the blood and bone marrow. It is characterized by the overproduction of immature white blood cells, known as myeloblasts or leukemic blasts, which do not function properly and can crowd out healthy cells. Detecting AML early can significantly impact treatment options […]
Symptoms and Testing information for Biopsy Breast Modified Radical Mastectomy and ER, PR, HER2NEU Test
Understanding the intricate procedures and the aftermath of breast cancer surgeries is crucial for patients navigating through their treatment journey. Among these procedures, the Biopsy Breast Modified Radical Mastectomy is a significant surgical method employed to combat breast cancer. This surgery involves the removal of the entire breast along with some lymph nodes under the […]
Symptoms and Testing information for Di-George Syndrome Karyotyping and FISH Test
— DiGeorge Syndrome, also known as 22q11.2 deletion syndrome, is a disorder caused by a defect in chromosome 22, leading to poor development of several bodily systems. This condition can result in a wide range of lifelong health issues, including heart defects, immune deficiencies, and developmental delays. Understanding the symptoms and undergoing the correct diagnostic […]
Symptoms and Testing information for Large Biopsy 6- Amputation Test
In the realm of medical diagnostics, the advancement of genetic testing has been a beacon of hope and clarity for many facing uncertain health conditions. Among these, the Large Biopsy 6- Amputation Test stands out as a pivotal assessment for individuals at risk of severe tissue damage necessitating amputation. DNA Labs UAE, a leading genetic […]
Symptoms and Testing information for Prader-Willi Syndrome Karyotyping and FISH Test
Prader-Willi Syndrome (PWS) is a rare genetic disorder that affects many parts of the body. Children and adults with PWS may experience a variety of symptoms, ranging from physical characteristics to behavioral issues. Understanding these symptoms is crucial for early diagnosis and treatment. DNA Labs UAE offers comprehensive testing for Prader-Willi Syndrome, including karyotyping and […]
Symptoms and Testing information for William’s Syndrome Karyotyping and FISH Test
Williams Syndrome is a rare genetic disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability or learning problems, unique personality characteristics, distinctive facial features, and heart and blood vessel (cardiovascular) problems. Recognizing the symptoms early can lead to better management of the condition. At DNA Labs […]