Ichthyosis congenital autosomal recessive type 1, also known as ARCI1, is a rare genetic condition that affects the skin. It is caused by mutations in the TGM1 gene, which plays a crucial role in the development of the skin’s outer layer. This condition is characterized by dry, thickened, scaly skin that can be present from […]
Ichthyosis with confetti, also known as ichthyosis en confetti or congenital reticular ichthyosiform erythroderma, is a rare skin disorder. It is characterized by red, scaly skin that is present from birth. Over time, individuals with this condition develop areas of normal skin amidst the widespread scaling, which resembles confetti. The primary gene associated with this […]
Symptoms of FLG Gene Ichthyosis Vulgaris Genetic Test Ichthyosis vulgaris is a common skin disorder caused by a mutation in the FLG gene, which affects the skin’s ability to retain moisture and protect against infections and allergens. This condition is characterized by dry, scaly skin that can range from mild to severe. Understanding the symptoms […]
Symptoms of SLC27A4 Gene Ichthyosis Prematurity Syndrome Ichthyosis prematurity syndrome (IPS) is a rare genetic condition that is caused by mutations in the SLC27A4 gene. This condition is characterized by a range of symptoms that primarily affect the skin, but can also impact other systems within the body. Understanding the symptoms of IPS is crucial […]
Ichthyosis follicularis, atrichia, and photophobia (IFAP) syndrome is a rare genetic condition that affects the skin, hair, and eyes. The syndrome is caused by mutations in the MBTPS2 gene. Individuals with this condition often experience a range of symptoms that can significantly impact their quality of life. DNA Labs UAE offers a comprehensive genetic test […]
Ichthyosis congenital, specifically the Harlequin fetus type, is a rare and severe genetic disorder that affects the skin. It is primarily caused by mutations in the ABCA12 gene, which plays a crucial role in the development of the skin’s lipid barrier. This condition is characterized by thick, hard, and deeply cracked skin, resembling the costume […]
Ichthyosis congenital autosomal recessive PNPLA1 related is a rare genetic condition that significantly affects the skin. Individuals with this condition have a mutation in the PNPLA1 gene, which plays a crucial role in the development and maintenance of healthy skin. This article delves into the symptoms of this genetic disorder and provides detailed information about […]
Understanding the complexities of genetic conditions is crucial for early diagnosis and effective management. One such condition is Ichthyosiform erythroderma congenital nonbullous type 1, caused by mutations in the NIPAL4 gene. This rare genetic disorder can lead to significant dermatological manifestations from birth or early childhood. At DNA Labs UAE, we provide comprehensive genetic testing […]
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals and families understand their genetic health. One of the specialized tests we offer is for the ALOXE3 gene, associated with Ichthyosiform Erythroderma Congenital Nonbullous Type 1 (IEC). This rare genetic condition can significantly impact the quality of life of […]
Understanding the complexities of genetic conditions is crucial for early diagnosis and management. One such condition, SOX18 Gene Hypotrichosis-lymphedema-telangiectasia syndrome, is a rare genetic disorder that impacts various body systems. It is characterized by a trio of primary symptoms: sparse hair (hypotrichosis), swelling caused by fluid accumulation (lymphedema), and small, dilated blood vessels near the […]
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.
