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Symptoms and Testing information for Amenorrhea Profile Test

At DNA Labs UAE, we understand the complexities and nuances of reproductive health. One of the specialized tests we offer is the Amenorrhea Profile Test, designed to delve into the potential causes behind amenorrhea, a condition characterized by the absence of menstrual periods in women of reproductive age. This comprehensive test, priced at 540 AED,

Symptoms and Testing information for Bacterial Meningitis Screen Test

Bacterial meningitis is a serious and potentially fatal condition that occurs when the protective membranes covering the brain and spinal cord, known as the meninges, become inflamed due to a bacterial infection. Early diagnosis and treatment are crucial for preventing severe health complications or death. DNA Labs UAE offers a comprehensive Bacterial Meningitis Screen Test

Symptoms and Testing information for Chromosome Analysis Cord Blood Test

Chromosome analysis, particularly through cord blood testing, is a crucial step in understanding the genetic blueprint of a newborn. This form of testing, offered by DNA Labs UAE, provides insights into the genetic makeup of an individual right from birth. The test, which costs 750 AED, is pivotal for detecting chromosomal abnormalities that could lead

Symptoms and Testing information for Canavan Disease Test

At DNA Labs UAE, we are committed to providing comprehensive genetic testing services, including the Canavan Disease Test. Canavan disease is a rare inherited disorder that affects the brain’s development. It falls under the category of leukodystrophies, diseases that impair the growth or maintenance of the myelin sheath, the protective covering of the nerve cells

Symptoms and Testing information for Galactosemia Panel 2 Test

At DNA Labs UAE, we understand the importance of early detection and management of genetic disorders. One such condition that requires immediate attention is Galactosemia. Our state-of-the-art genetic laboratory offers a comprehensive Galactosemia Panel 2 Test, designed to detect various forms of this genetic disorder. This test is a crucial step in diagnosing the condition

Symptoms and Testing information for Galactosemia Panel 3 Test

Galactosemia is a rare genetic disorder that affects an individual’s ability to metabolize galactose, a sugar found in milk and other dairy products. This condition can lead to various health issues if not diagnosed and managed properly. DNA Labs UAE offers a comprehensive Galactosemia Panel 3 Test to identify this condition early on, ensuring that

Symptoms and Testing information for Sphingolipidosis Panel 2 Test

Sphingolipidoses represent a group of inherited metabolic disorders characterized by the accumulation of sphingolipids in tissues, due to defects in their breakdown. These disorders can lead to various physical and neurological symptoms, depending on the specific type of sphingolipidosis. DNA Labs UAE offers a comprehensive Sphingolipidosis Panel 2 Test, designed to diagnose these complex genetic

Symptoms and Testing information for Amino Acids Maple Syrup Urine Disease MSUD Panel Plasma Test

In the realm of genetic disorders, Maple Syrup Urine Disease (MSUD) stands out due to its unique name and the serious health implications it poses. This inherited disorder affects the body’s ability to break down certain amino acids, leading to a buildup that can be harmful. At DNA Labs UAE, we are committed to providing

Symptoms and Testing information for Newborn Screening Panel Extended Test

In the dynamic field of genetics and neonatal care, the Newborn Screening Panel Extended Test stands out as a crucial tool for early detection of potential health issues in newborns. This comprehensive test, available at DNA Labs UAE for a cost of 1000 AED, is designed to screen for a wide range of genetic, hormonal,

Symptoms and Testing information for Sphingolipidosis Panel 3 Test

Sphingolipidosis represents a group of lysosomal storage disorders characterized by the accumulation of sphingolipids in tissues due to defects in their breakdown. These disorders are caused by genetic mutations that affect the enzymes responsible for the metabolism of sphingolipids. The Sphingolipidosis Panel 3 Test is a comprehensive diagnostic tool designed to detect genetic mutations associated

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