Blogs

— Understanding the GFM2 Gene Microcephaly with Simplified Gyral Pattern and Insulin-Dependent Diabetes In the realm of genetic testing and diagnostics, DNA Labs UAE stands at the forefront, offering a wide array of genetic tests designed to uncover and understand various genetic conditions. Among these, the test for GFM2 Gene Microcephaly with Simplified Gyral Pattern […]

Symptoms of KIF11 Gene Microcephaly with or without Chorioretinopathy, Lymphedema, or Mental Retardation (MCLMR) Genetic Test Understanding the symptoms associated with KIF11 Gene Microcephaly with or without Chorioretinopathy, Lymphedema, or Mental Retardation (MCLMR) is crucial for early diagnosis and management of this rare genetic disorder. The KIF11 gene plays a significant role in cell division […]

Microcephaly with epilepsy and diabetes syndrome (MEDS), also known as IER3IP1 syndrome, is a rare genetic condition that presents a complex array of symptoms affecting various systems within the body. This condition is attributed to mutations in the IER3IP1 gene, which plays a significant role in the development and function of the nervous system and […]

Microcephaly with cortical malformations, Autosomal Recessive Type 2, is a rare genetic disorder caused by mutations in the WDR62 gene. This condition is characterized by significantly reduced head size (microcephaly) and abnormalities in the cerebral cortex, the part of the brain responsible for many important functions including memory, attention, perceptual awareness, thought, language, and consciousness. […]

Microcephaly and chorioretinopathy are conditions that can have a profound impact on an individual’s quality of life. These conditions can occur either with or without associated mental retardation. Recent advances in genetic research have identified the TUBGCP6 gene as a critical factor in the development of these conditions. At DNA Labs UAE, we offer a […]

In the realm of genetic testing, understanding the nuances of specific conditions is crucial for early diagnosis and management. Among these conditions, Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD II), caused by mutations in the PCNT gene, stands out due to its rarity and the complexity of its symptoms. At DNA Labs UAE, we offer […]

Metaphyseal anadysplasia type 2, caused by mutations in the MMP9 gene, is a rare genetic disorder characterized by skeletal abnormalities. DNA Labs UAE offers a comprehensive genetic test for this condition, providing crucial information for affected individuals and their families. Understanding the symptoms associated with this disorder is essential for early diagnosis and management. Symptoms […]

Understanding the complexities of genetic conditions is crucial for early diagnosis and effective management. One such condition that has garnered attention in the medical community is Metaphyseal Anadysplasia Type 1, associated with mutations in the MMP13 gene. This condition, although rare, can have significant implications for affected individuals and their families. DNA Labs UAE is […]

Symptoms of HUWE1 Gene Mental Retardation X-Linked Syndromic Turner Type Genetic Test The HUWE1 gene plays a critical role in the development and function of the nervous system. Mutations in this gene are associated with a condition known as Mental Retardation X-Linked Syndromic Turner type (MRXSLT). This condition is characterized by a range of neurological […]

In the realm of medical genetics, understanding the intricate web of genes and their impact on health is a constantly evolving field. One such area of focus is the INPP5E gene and its associated conditions. This gene plays a crucial role in the development and function of various bodily systems, and mutations in this gene […]