Understanding the genetic underpinnings of various conditions is crucial for accurate diagnosis and effective management. Among these, the ZC4H2 gene plays a significant role in the development of Wieacker-Wolff Syndrome, a rare X-linked recessive disorder. DNA Labs UAE offers a comprehensive genetic test for this condition, priced at 4400 AED, aimed at identifying mutations in […]
Wilson-Turner syndrome is a rare genetic disorder that primarily affects males. It is characterized by intellectual disability, obesity, gynecomastia (enlarged breasts in males), and hypogonadism (decreased function of the gonads). This condition is caused by mutations in the LAS1L gene, which plays a crucial role in the normal development and function of various systems in […]
Symptoms of PEX1 Gene Zellweger Syndrome Genetic Test Zellweger Syndrome, a rare congenital disorder, falls under the spectrum of Peroxisome Biogenesis Disorders (PBDs), which are characterized by the impairment of peroxisomes. These cellular organelles play a pivotal role in the metabolism of certain types of fatty acids and are crucial for the brain and liver’s […]
— Zellweger Syndrome is a rare, inherited disorder that is part of a group of diseases known as peroxisome biogenesis disorders (PBDs), which are characterized by the reduction or absence of functional peroxisomes in the cells of the body. The PEX10 gene plays a crucial role in the assembly of peroxisomes, and mutations in this […]
Zellweger Syndrome, a rare and inherited condition, falls under a group of disorders known as peroxisome biogenesis disorders (PBDs), which are part of a larger set of diseases known as leukodystrophies. These conditions affect the white matter of the brain and also impact the function of peroxisomes – essential cellular structures that help break down […]
Zellweger Syndrome is a rare, inherited disorder that disrupts the normal functions of the cell’s peroxisomes. These are structures in cells that help break down toxic substances and synthesize lipids necessary for cell membrane integrity. The PEX13 gene plays a crucial role in the formation and function of peroxisomes. Mutations in the PEX13 gene can […]
Zellweger Syndrome is a rare genetic disorder that belongs to a group of diseases known as peroxisome biogenesis disorders (PBD), which are part of a larger collection of diseases referred to as leukodystrophies. These disorders affect the myelin sheath, a fatty covering that acts as an insulator around nerve fibers in the brain. One of […]
Symptoms of PEX16 Gene Zellweger Syndrome Genetic Test Zellweger Syndrome is a rare, inherited disorder that is part of a group of diseases known as peroxisome biogenesis disorders (PBDs), within the larger family of leukodystrophies. These diseases affect the myelin sheath, a fatty covering that acts as an insulator around nerve fibers in the brain. […]
Symptoms of PEX19 Gene Zellweger Syndrome Genetic Test Zellweger Syndrome represents a spectrum of rare, inherited, metabolic disorders known as peroxisome biogenesis disorders (PBDs), which are part of the larger family of leukodystrophies. These disorders affect the body’s ability to create and maintain peroxisomes, which are cellular structures essential for the normal functioning of cell […]
Zellweger Syndrome represents a spectrum of rare, congenital disorders characterized by the absence or malfunction of peroxisomes in the cells of the liver, kidneys, and brain. Among the genes implicated in this condition, mutations in the PEX2 gene are a known cause. DNA Labs UAE offers a comprehensive genetic test for the PEX2 gene mutation, […]
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.
