Understanding FKRP Gene Muscular Dystrophy Type 1C Muscular dystrophies are a group of genetic diseases characterized by progressive weakness and degeneration of the skeletal muscles that control movement. Among these, FKRP gene muscular dystrophy type 1C, also known as LGMD2I, is a rare form that is caused by mutations in the FKRP gene. This condition […]
Muscular dystrophy encompasses a group of genetic diseases characterized by progressive weakness and degeneration of the skeletal muscles that control movement. Among these, LAMA2-related muscular dystrophy, specifically type 1A, is caused by mutations in the LAMA2 gene. This condition has garnered attention within the medical community due to its significant impact on individuals’ quality of […]
Symptoms of POMK Gene Muscle-Eye-Brain Disease Muscle-Eye-Brain (MEB) disease is a rare genetic disorder that affects the development of the muscles, eyes, and brain. This condition is caused by mutations in the POMK gene. The symptoms of MEB disease can vary significantly from one individual to another but generally include a combination of muscular, ocular, […]
In the realm of genetic testing, the MSTN gene muscle hypertrophy genetic test stands out for its unique ability to identify individuals who have a genetic predisposition to developing increased muscle mass. This condition, known as muscle hypertrophy, can have a significant impact on an individual’s physical capabilities and overall health. At DNA Labs UAE, […]
ACTA2 gene multisystemic smooth muscle dysfunction syndrome is a rare genetic disorder that affects multiple organ systems within the body. This condition is characterized by a wide range of symptoms, due to the critical role that the ACTA2 gene plays in the function of smooth muscle cells. These cells are found throughout the body, including […]
Understanding ISCA2 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 4 Mitochondrial diseases are a complex group of disorders that affect the mitochondria, the powerhouse of the cell. One such rare and severe condition is Multiple Mitochondrial Dysfunctions Syndrome Type 4 (MMDS4), caused by mutations in the ISCA2 gene. This condition has a profound impact on an […]
Symptoms of IBA57 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 3 Genetic Test Multiple Mitochondrial Dysfunctions Syndrome Type 3 (MMDS3) is a rare genetic disorder caused by mutations in the IBA57 gene. This condition affects various systems in the body, leading to a wide range of symptoms that can significantly impact the quality of life of […]
In the ever-evolving field of genetics, understanding the complexities of various syndromes and conditions is crucial for early diagnosis and management. One such condition that has garnered attention in recent years is Multiple Mitochondrial Dysfunctions Syndrome Type 2 (MMDS2), caused by mutations in the BOLA3 gene. DNA Labs UAE is at the forefront of providing […]
Understanding the symptoms of NFU1 Gene Multiple Mitochondrial Dysfunctions Syndrome Type 1 (MMDS1) is crucial for early diagnosis and management of this rare but serious condition. This genetic disorder, caused by mutations in the NFU1 gene, affects mitochondrial function, leading to a range of systemic symptoms. At DNA Labs UAE, we offer a comprehensive genetic […]
Understanding the nuances of genetic disorders is pivotal in the realm of modern medicine, particularly when it comes to diagnosing and managing rare syndromes. One such complex condition is the PIGT Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 3 (PIGT-MCAHS3). This genetic disorder, though rare, presents a spectrum of symptoms that can significantly impact the quality […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
