Pneumology Diseases

Understanding the genetic underpinnings of various syndromes is crucial for early diagnosis and management. One such rare but significant condition is the TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome (SIDDT). This condition, linked to mutations in the TSPYL1 gene, has garnered attention due to its severe implications, including sudden infant death […]

In the realm of genetic testing, advancements have paved the way for identifying and understanding a plethora of genetic conditions that affect individuals from birth. Among these, anomalies related to the GATA4 gene stand out due to their significant impact on individuals’ health, particularly concerning testicular anomalies with or without congenital heart disease. At DNA […]

In the realm of genetic testing and diagnosis, advancements have been pivotal in identifying and managing congenital heart defects, one of which is the Tetralogy of Fallot (TOF). At the forefront of these advancements is the ALDH1A2 gene Tetralogy of Fallot genetic test, a specialized diagnostic tool designed to detect mutations associated with TOF. DNA […]

The GATA6 gene is crucial for the development of various organs in the body, including the pancreas and heart. Mutations in this gene can lead to pancreatic agenesis and congenital heart defects, conditions that are both serious and potentially life-threatening. Understanding the symptoms associated with these conditions and the importance of genetic testing can be […]

McKusick-Kaufman syndrome (MKKS), also known as Kaufman-McKusick syndrome, is a rare genetic disorder that affects multiple systems of the body. This condition is inherited in an autosomal recessive pattern, meaning that an individual must receive a defective gene from each parent to be affected. The MKKS gene, which plays a crucial role in the development […]

In the realm of genetic testing, advancements have paved the way for early detection and intervention in numerous hereditary conditions. Among these, the TRPM4 gene-related progressive familial heart block stands out due to its critical impact on cardiac health. DNA Labs UAE is at the forefront of this pioneering field, offering a comprehensive genetic test […]

At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals and families understand their genetic makeup and potential health risks. One of the critical tests we offer is for the MT-TC Gene MELAS Syndrome. This condition, which stands for Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes, is a rare […]

In the realm of genetic testing and diagnosis, understanding the intricacies of specific genes and their associated conditions is crucial for both patients and healthcare providers. One such condition that has garnered attention is Idiopathic Pulmonary Fibrosis (IPF), a chronic and ultimately fatal disease characterized by a progressive decline in lung function. The SFTPA1 gene […]

MELAS syndrome, which stands for Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes, is a complex genetic condition that affects various systems of the body, particularly the nervous system and muscles. It is caused by mutations in mitochondrial DNA, specifically in the MT-TF gene. Understanding the symptoms of MELAS syndrome is crucial for early diagnosis and […]

Pulmonary hypertension in newborns, also known as neonatal pulmonary hypertension, is a serious and potentially life-threatening condition characterized by high blood pressure in the lungs’ arteries. This condition can significantly impact the oxygenation of the newborn’s body, leading to critical health issues. Recent advancements in genetic research have identified a connection between the CRHR1 gene […]