Understanding COA5 Gene Cardioencephalomyopathy Fatal Infantile Due to Cytochrome C Oxidase Deficiency Type 3 Cardioencephalomyopathy fatal infantile due to cytochrome c oxidase deficiency type 3, caused by mutations in the COA5 gene, is a rare and severe condition that primarily affects infants. This genetic disorder disrupts the normal function of mitochondria, the energy-producing structures within […]
Pneumology Diseases
Symptoms and Testing information for TIMP1 Gene Bicuspid Aortic Valve Genetic Test
Understanding the genetic underpinnings of heart conditions can significantly impact the approach to prevention, diagnosis, and treatment. Among these conditions, the Bicuspid Aortic Valve (BAV) disorder stands out due to its prevalence and potential complications. Recent advancements in genetic testing, particularly concerning the TIMP1 gene, have paved the way for early detection and management strategies. […]
Symptoms and Testing information for SCN5A Gene Brugada Syndrome Type 1 Genetic Test
Understanding the nuances and implications of genetic conditions is essential for both medical professionals and patients. One such condition that has garnered attention is Brugada Syndrome Type 1, a disorder that affects the heart’s rhythm. It’s crucial to recognize the symptoms of this condition early on, as it can lead to serious heart complications, including […]
Symptoms and Testing information for ABCC9 Gene Atrial Fibrillation Type 12 Genetic Test
Understanding the genetic underpinnings of atrial fibrillation (AF) can provide crucial insights into its diagnosis, management, and treatment. One such genetic marker linked to the condition is the ABCC9 gene, which has been associated with Atrial Fibrillation Type 12. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the ABCC9 […]
Symptoms and Testing information for KCNQ1 Gene Atrial Fibrillation Type 3 Genetic Test
Understanding the nuances of genetic conditions is crucial in today’s healthcare landscape. Among these conditions, Atrial Fibrillation (AF) stands out due to its prevalence and potential complications. A particular form of this condition, Type 3 Atrial Fibrillation, is genetically linked to mutations in the KCNQ1 gene. This article delves into the symptoms associated with this […]
Symptoms and Testing information for KCNE2 Gene Atrial Fibrillation Type 4 Genetic Test
Understanding the intricacies of our genetic makeup is pivotal in diagnosing, treating, and potentially preventing numerous health conditions. One such condition that has garnered attention in the medical community is Atrial Fibrillation Type 4, associated with mutations in the KCNE2 gene. DNA Labs UAE is at the forefront of offering comprehensive genetic testing services, including […]
Symptoms and Testing information for NPPA Gene Atrial Fibrillation Type 6 Genetic Test
Understanding Atrial Fibrillation Type 6 and the Role of the NPPA Gene Atrial Fibrillation (AF) is the most common form of serious arrhythmia, affecting millions of individuals worldwide. It’s characterized by rapid and irregular heartbeats that can lead to a range of complications, including stroke, heart failure, and other heart-related problems. Among the various types […]
Symptoms and Testing information for KCNA5 Gene Atrial Fibrillation Type 7 Genetic Test
Atrial Fibrillation (AF) is a common type of arrhythmia, or irregular heartbeat, which can lead to blood clots, stroke, heart failure, and other heart-related complications. The discovery of genetic factors contributing to AF has opened new doors for understanding and managing this condition. Among these genetic factors, mutations in the KCNA5 gene have been identified […]
Symptoms and Testing information for MYH6 Gene Atrial Septal Defect Type 3 Genetic Test
Understanding the symptoms and genetic predispositions to certain conditions is crucial for early diagnosis and effective treatment. Atrial Septal Defect Type 3 (ASD3), a congenital heart defect characterized by a hole in the wall (septum) that divides the upper chambers (atria) of the heart, is one such condition that can have significant implications for an […]
Symptoms and Testing information for TGFB3 Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 1 Genetic Test
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Type 1 is a complex genetic condition that affects the heart’s muscle tissue, leading to arrhythmias and heart failure. The TGFB3 gene has been identified as one of the genetic contributors to this condition. Understanding the symptoms and seeking early diagnosis through genetic testing can be crucial in managing and […]