Limb-girdle muscular dystrophy (LGMD) is a group of genetic disorders characterized by progressive muscle weakness and atrophy, primarily affecting the shoulder and pelvic girdles. Among the various subtypes, LGMD autosomal recessive type 2A, caused by mutations in the CAPN3 gene, is one of the most common. The CAPN3 gene provides instructions for producing a protein […]
Limb-girdle muscular dystrophy (LGMD) is a term for a group of diseases that cause weakness and wasting of the muscles in the arms and legs. The muscles most affected are those closest to the body (proximal muscles), specifically the muscles of the shoulders, upper arms, pelvic area, and thighs. The severity, age of onset, and […]
Limb-girdle muscular dystrophy (LGMD) is a genetically and clinically heterogeneous group of rare muscular dystrophies. It is characterized by progressive weakness and wasting of the muscles around the hips and shoulders, which constitute the limb girdle area. Among the various types of LGMD, autosomal recessive type 2F, caused by mutations in the SGCD gene, is […]
Limb-girdle muscular dystrophy (LGMD) is a term for a group of diseases that cause weakness and wasting of the muscles in the arms and legs. The muscles most affected are those closest to the body (proximal muscles), specifically the muscles of the shoulders, upper arms, pelvic area, and thighs. The severity, age of onset, and […]
Limb-girdle muscular dystrophy (LGMD) is a term for a group of diseases that cause weakness and wasting of the muscles in the arms and legs. The muscles most affected are those closest to the body (proximal muscles), specifically the muscles of the shoulders, upper arms, pelvic area, and thighs. The severity, age of onset, and […]
Limb-girdle muscular dystrophy (LGMD) is a term for a group of diseases that cause weakness and wasting of the muscles in the arms and legs. The muscles most affected are those closest to the body (proximal muscles), specifically the muscles of the shoulders and upper arms and the muscles of the hips and thighs. LGMD […]
Limb-girdle muscular dystrophy (LGMD) represents a diverse group of genetic disorders characterized by progressive weakness and wasting of the muscles, particularly those around the hips and shoulders, known as the limb-girdle area. Among the various subtypes of LGMD, autosomal dominant type 1A, linked to mutations in the MYOT gene, stands out for its distinct clinical […]
Lewy body dementia (LBD) is a complex, progressive brain disorder that affects an individual’s ability to think, reason, and move. It shares symptoms with other more common diseases like Alzheimer’s and Parkinson’s, making it challenging to diagnose accurately. However, advancements in genetics have opened new doors to understanding the susceptibility to LBD, particularly through the […]
At DNA Labs UAE, we are committed to providing our clients with comprehensive and accurate genetic testing services. Among the various tests we offer, the AARS2 Gene Leukoencephalopathy Progressive with Ovarian Failure Genetic Test is particularly significant for individuals showing symptoms of this rare but impactful condition. Understanding the symptoms and undergoing timely testing can […]
Understanding CSF1R Gene Leukoencephalopathy CSF1R gene leukoencephalopathy, also known as diffuse hereditary leukoencephalopathy with spheroids (HDLS), is a rare genetic disorder affecting the brain. This condition is characterized by changes in the white matter of the brain, leading to a wide range of neurological symptoms. The disease is caused by mutations in the CSF1R gene, […]
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.
