Symptoms and Testing information for Methylenetetrahydrofolate Reductase MTHFR - 2 Variants C677T A1298C Test

Symptoms and Testing information for Methylenetetrahydrofolate Reductase MTHFR – 2 Variants C677T A1298C Test

Understanding the intricacies of our genetic makeup is key to unraveling the mysteries of various health conditions that affect us. One such genetic aspect that has garnered attention in recent years is the Methylenetetrahydrofolate Reductase (MTHFR) gene and its variants, specifically C677T and A1298C. These genetic variants can significantly impact bodily functions, particularly those related […]

Symptoms and Testing information for NPM1 Mutation Analysis Exon 12 Insertion Test

Symptoms and Testing information for NPM1 Mutation Analysis Exon 12 Insertion Test

— The NPM1 mutation, particularly the Exon 12 insertion, is a significant biomarker in the diagnosis and management of acute myeloid leukemia (AML). Understanding the symptoms that necessitate the NPM1 Mutation Analysis Exon 12 Insertion Test is crucial for early detection and treatment. This test, offered by DNA Labs UAE for 1200 AED, is a […]

Symptoms and Testing information for QF PCR Panel 131821XY Test

Symptoms and Testing information for QF PCR Panel 131821XY Test

In the realm of genetic testing, the QF PCR Panel 131821XY Test stands out as a critical tool for diagnosing various chromosomal abnormalities. This test, available at DNA Labs UAE, is specifically designed to detect anomalies in chromosomes 13, 18, 21, and the sex chromosomes (X and Y), which are associated with several genetic disorders. […]

Symptoms and Testing information for RUNX1-RUNX1T1 AML1- ETO t8;21 Quantitative Test

Symptoms and Testing information for RUNX1-RUNX1T1 AML1- ETO t8;21 Quantitative Test

Acute myeloid leukemia (AML) with t(8;21)(q22;q22) translocation, characterized by the fusion of the RUNX1 (AML1) gene on chromosome 21 and the RUNX1T1 (ETO) gene on chromosome 8, is a distinct subtype of AML recognized for its unique clinical and pathological features. This subtype, often referred to as RUNX1-RUNX1T1 AML or AML1-ETO t(8;21), represents approximately 8-15% […]

Symptoms and Testing information for Beta Thalassemia Screening Prenatal Test

Symptoms and Testing information for Beta Thalassemia Screening Prenatal Test

Beta thalassemia is a blood disorder that reduces the production of hemoglobin, the iron-containing protein in red blood cells that carries oxygen to cells throughout the body. It is a genetic condition that can lead to anemia, a condition characterized by fatigue and weakness due to the lack of healthy red blood cells. Screening for […]

Symptoms and Testing information for Chromosomes 13 and 21 Test

Symptoms and Testing information for Chromosomes 13 and 21 Test

DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services to help individuals understand their genetic makeup and the implications it may have on their health and wellbeing. Among the various tests offered, the Chromosomes 13 and 21 Test is particularly noteworthy for its importance in detecting […]

Symptoms and Testing information for Chromosomes 18 X and Y Test

Symptoms and Testing information for Chromosomes 18 X and Y Test

In the realm of genetic testing, understanding the nuances of our genetic makeup is crucial for diagnosing various conditions and diseases. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the Chromosomes 18, X, and Y test. This test plays a pivotal role in diagnosing and understanding disorders linked to […]

Symptoms and Testing information for Cord Blood for Karyotyping Test

Symptoms and Testing information for Cord Blood for Karyotyping Test

At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help families understand their genetic makeup and identify potential health risks. One of the critical tests we offer is the Cord Blood for Karyotyping Test. This test is instrumental in detecting chromosomal abnormalities that could affect a child’s health. Understanding the […]

Symptoms and Testing information for Cystic Fibrosis Mutation Screening CFTR - Del 508 Test

Symptoms and Testing information for Cystic Fibrosis Mutation Screening CFTR – Del 508 Test

Cystic Fibrosis (CF) is a genetic disorder that affects the respiratory, digestive, and reproductive systems, leading to severe symptoms that can impact the quality of life. It is caused by mutations in the CFTR gene, with the Delta F508 (Del 508) mutation being the most common. Understanding the symptoms and undergoing mutation screening can help […]

Symptoms and Testing information for Sanger Sequencing Single Variant Test

Symptoms and Testing information for Sanger Sequencing Single Variant Test

Understanding the Sanger Sequencing Single Variant Test The Sanger Sequencing Single Variant Test is a specialized diagnostic tool utilized in the realm of genetic testing. This method, developed by Frederick Sanger and his colleagues in 1977, remains a gold standard for the accurate detection of specific genetic variants. DNA Labs UAE is at the forefront […]

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