Fragile X-associated tremor/ataxia syndrome (FXTAS) is a genetic condition that primarily affects older adults, leading to problems with movement, cognition, and daily functioning. This disorder is linked to mutations in the FMR1 gene, which is also associated with Fragile X syndrome, the most common form of inherited intellectual disability. Understanding the symptoms and undergoing genetic […]

Fragile X Syndrome (FXS) is a genetic condition that causes a range of developmental problems, including learning disabilities and cognitive impairment. It is the most common form of inherited intellectual disability in males and a significant cause of intellectual disability in females. The condition is linked to mutations in the FMR1 gene, which plays a […]

At DNA Labs UAE, we are committed to providing advanced genetic testing services that cater to a wide range of genetic conditions. One such condition is Filaminopathy, a group of genetic disorders caused by mutations in the FLNC gene. Understanding the symptoms of FLNC gene Filaminopathy is crucial for early diagnosis and management. This article […]

Understanding the complexities of genetic disorders is crucial for early diagnosis and intervention. Among these, FG Syndrome Type 4, linked to mutations in the CASK gene, is a condition that warrants attention. At DNA Labs UAE, we offer a comprehensive CASK Gene FG Syndrome Type 4 Genetic Test designed to provide accurate diagnoses for individuals […]

FG Syndrome Type 2 is a rare genetic disorder that has been linked to mutations in the FLNA gene. This condition primarily affects males and can lead to a wide range of physical and developmental challenges. Understanding the symptoms associated with this syndrome is crucial for early diagnosis and management. DNA Labs UAE offers a […]

Symptoms of MED12 Gene FG Syndrome Type 1 Genetic Test FG Syndrome Type 1, a rare genetic condition, has been a subject of study and concern within the medical community. This condition, caused by mutations in the MED12 gene, can lead to a variety of developmental and physical challenges. Understanding the symptoms and the importance […]

Febrile seizures are convulsions brought on by a fever in infants and young children. While they can be alarming for parents, they are typically benign. However, a subset of febrile seizures known as Familial Febrile Seizures Type 4 are linked to mutations in the ADGRV1 gene. Understanding the symptoms and genetic underpinnings of this condition […]

— Symptoms of PRNP Gene Fatal Familial Insomnia Genetic Test Fatal Familial Insomnia (FFI) is a rare genetic disorder that affects the brain, leading to severe insomnia and a range of other neurological symptoms. This condition is caused by a mutation in the PRNP gene, which plays a crucial role in the production of prion […]

Understanding the complexities of genetic conditions is crucial for both patients and their families. One such condition that has garnered attention in the medical community is Familial Infantile Myoclonic Epilepsy (FIME), a disorder associated with mutations in the TBC1D24 gene. Recognizing the symptoms of this condition early on can significantly impact the management and outcome […]

Familial Hemiplegic Migraine (FHM) is a rare form of migraine headache that, unlike typical migraines, involves some degree of paralysis (hemiplegia) during the episode. Type 3 Familial Hemiplegic Migraine (FHM3) is specifically linked to mutations in the SCN1A gene. Recognizing the symptoms and understanding the genetic underpinnings of this condition is crucial for effective management […]