Lissencephaly, meaning “smooth brain,” is a rare, gene-linked brain malformation characterized by the absence of normal convolutions (folds) in the cerebral cortex and an abnormally small head (microcephaly). Among the various types of lissencephaly, Type 5, associated with mutations in the LAMB1 gene, presents a unique set of challenges and symptoms for affected individuals and […]
Symptoms of AKT3 Gene Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome Type 2 Genetic Test Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus (MPPH) Syndrome Type 2 is a rare genetic disorder primarily affecting the development of the brain. This condition is characterized by several key features, including an abnormally large brain (megalencephaly), irregularities in the brain’s surface (polymicrogyria), extra fingers or toes (polydactyly), and an accumulation […]
Understanding the symptoms associated with DCX Gene Lissencephaly X-Linked Type 1 is crucial for early diagnosis and management of the condition. DNA Labs UAE offers comprehensive genetic testing for this condition, which can be a critical step in managing and understanding this complex neurological disorder. Symptoms of DCX Gene Lissencephaly X-Linked Type 1 Lissencephaly, which […]
Meier-Gorlin syndrome (MGS) is a rare genetic disorder characterized by a spectrum of clinical features, including primordial dwarfism, microcephaly, and skeletal abnormalities. Among the genes associated with this condition, mutations in the ORC1 gene lead to Meier-Gorlin Syndrome Type 1. Recognizing the symptoms associated with this particular type of MGS is crucial for early diagnosis […]
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals and families understand their genetic makeup and manage their health proactively. One of the critical tests we offer is the ARX Gene Lissencephaly X-Linked Type 2 Genetic Test. This test is crucial for diagnosing a rare genetic disorder that […]
Meier-Gorlin Syndrome (MGS) is a rare genetic disorder that is primarily characterized by short stature, small ears, and absent or underdeveloped kneecaps (patellae). Among the various genes associated with this condition, mutations in the ORC4 gene result in Meier-Gorlin Syndrome Type 2. Recognizing the symptoms associated with this specific type is crucial for early diagnosis […]
Symptoms of MED12 Gene Lujan-Fryns Syndrome Genetic Test Lujan-Fryns syndrome (LFS) is a rare genetic disorder that primarily affects males, though females can be carriers of the condition. It is associated with mutations in the MED12 gene, located on the X chromosome. This condition is characterized by a variety of physical, behavioral, and cognitive features. […]
Lymphedema-Distichiasis Syndrome (LDS) is a rare, genetic condition that is often underdiagnosed due to its variable presentation and the subtlety of its early symptoms. This condition is caused by mutations in the FOXC2 gene, which plays a crucial role in the development and function of the lymphatic system. Understanding the symptoms of this condition is […]
DNA Labs UAE is at the forefront of genetic testing, offering a wide range of services designed to provide valuable insights into your genetic makeup and potential health risks. One of the specialized tests offered by DNA Labs UAE is the RIN2 Gene Macrocephaly Alopecia Cutis Laxa and Scoliosis Genetic Test. This comprehensive test is […]
Understanding POLD1 Gene Mandibular Hypoplasia Deafness Progeroid Features and Lipodystrophy Syndrome POLD1 Gene Mandibular Hypoplasia Deafness Progeroid Features and Lipodystrophy Syndrome, commonly abbreviated as MDPL Syndrome, is a rare genetic disorder that presents a constellation of symptoms. This condition is caused by mutations in the POLD1 gene, which plays a crucial role in DNA replication […]
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.
