The HOXD13 gene plays a crucial role in the development of limbs and digits in the human body. Mutations in this gene can lead to a condition known as Brachydactyly Type E1, a rare genetic disorder characterized by the shortening of bones in the hands and feet, which can significantly affect the functionality and appearance […]
Symptoms of SLC20A2 Gene Basal Ganglia Calcification Type 1 Ideopathic Genetic Test The SLC20A2 gene plays a pivotal role in phosphate regulation within the human body, and mutations in this gene can lead to Basal Ganglia Calcification Type 1, also known as Idiopathic Basal Ganglia Calcification (IBGC1) or Fahr’s Disease. This condition is characterized by […]
Understanding the intricate nature of our genetics has always been a cornerstone of medical science. It is through this understanding that we can uncover the mysteries behind various genetic disorders, one of which is the PDGFRB Gene Basal Ganglia Calcification Type 4. This condition, while rare, can have a significant impact on those affected. DNA […]
Understanding the symptoms of PDGFB Gene Basal Ganglia Calcification Type 5 Idiopathic and the significance of genetic testing for this condition is crucial for early diagnosis and management. PDGFB Gene Basal Ganglia Calcification Type 5, also known as Idiopathic Basal Ganglia Calcification (IBGC) Type 5, is a genetic disorder characterized by the abnormal accumulation of […]
Understanding XPR1 Gene Basal Ganglia Calcification Type 6 Ideopathic Genetic Test Basal Ganglia Calcification (BGC) is a rare neurological disorder characterized by abnormal deposits of calcium in certain areas of the brain, including the basal ganglia. These deposits can lead to a range of neurological symptoms. Type 6 Basal Ganglia Calcification, associated with mutations in […]
Understanding the symptoms of UPB1 gene beta-ureidopropionase deficiency is critical for early diagnosis and management of this rare genetic disorder. At DNA Labs UAE, we provide a comprehensive genetic test for this condition, aimed at identifying mutations in the UPB1 gene that can lead to beta-ureidopropionase deficiency. This article will delve into the symptoms associated […]
Understanding the intricacies of genetic conditions is crucial for early diagnosis and treatment. One such condition that has garnered attention in the medical community is related to the FREM1 gene, which can lead to a bifid nose – a rare congenital anomaly. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, […]
Auriculocondylar syndrome (ACS) represents a rare genetic condition, with Auriculocondylar Syndrome Type 1 being one of its forms, primarily resulting from mutations in the GNAI3 gene. This syndrome is characterized by a range of physical malformations that primarily affect the structure of the patient’s face. DNA Labs UAE offers a comprehensive genetic test for those […]
Birt-Hogg-Dubé (BHD) syndrome is a rare genetic condition that is often misunderstood or misdiagnosed due to the variety of symptoms it presents. Caused by mutations in the FLCN gene, this syndrome can lead to skin lesions, lung cysts, spontaneous pneumothorax, and an increased risk of developing certain types of tumors, particularly in the kidneys. Understanding […]
Auriculocondylar Syndrome Type 2 (ACS2) is a rare genetic disorder that affects the development of the ear, mandible (jawbone), and in some cases, the heart. This condition is primarily caused by mutations in the PLCB4 gene, which plays a crucial role in the development of these structures. Recognizing the symptoms of ACS2 is vital for […]
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.
