Symptoms of GALC Gene Krabbe Disease Krabbe disease, also known as globoid cell leukodystrophy, is a rare and often severe disorder that affects the nervous system. It is caused by mutations in the GALC gene, which leads to a deficiency in an enzyme necessary for the metabolism of certain lipids in the body. This deficiency […]
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Symptoms and Testing information for ROGDI Gene Kohlschutter Tonz syndrome Genetic Test
Symptoms of ROGDI Gene Kohlschutter Tonz Syndrome Genetic Test Kohlschutter Tonz Syndrome is a rare genetic disorder that impacts the neurological system and dental health. It is characterized by epilepsy, developmental delay, and amelogenesis imperfecta, a condition affecting dental enamel. This disorder is caused by mutations in the ROGDI gene, and understanding its symptoms is […]
Symptoms and Testing information for RYR1 Gene King-Denborough syndrome Genetic Test
Symptoms of RYR1 Gene King-Denborough Syndrome Genetic Test King-Denborough Syndrome (KDS) is a rare genetic condition, characterized by distinct physical features, muscle weakness, and susceptibility to malignant hyperthermia, a severe reaction to certain anesthesia drugs. This condition is primarily associated with mutations in the RYR1 gene, which plays a critical role in muscle contraction. Understanding […]
Symptoms and Testing information for FAM111A Gene Kenny-Caffey syndrome type 2 Genetic Test
In the realm of genetic testing and diagnosis, advancements have made it possible to identify and understand a myriad of genetic disorders that affect individuals from birth. Among these, Kenny-Caffey Syndrome Type 2 (KCS2) stands out due to its rarity and the specific challenges it presents. Caused by mutations in the FAM111A gene, KCS2 is […]
Symptoms and Testing information for KDM6A Gene Kabuki syndrome type 2 Genetic Test
Kabuki syndrome, a rare, multisystem disorder, is characterized by distinctive facial features, growth delays, skeletal abnormalities, and a range of other clinical manifestations. While Kabuki syndrome type 1 has been widely recognized, advancements in genetic testing have led to the identification of Kabuki syndrome type 2, caused by mutations in the KDM6A gene. Recognizing the […]
Symptoms and Testing information for EXOSC8 Gene Joubert syndrome EXOSC8 related Genetic Test
Symptoms of EXOSC8 Gene Joubert Syndrome Joubert Syndrome is a rare genetic disorder that affects the development of the cerebellum, a part of the brain that controls balance and coordination. This disorder is associated with mutations in several genes, including the EXOSC8 gene. The symptoms of Joubert Syndrome can vary significantly among affected individuals but […]
Symptoms and Testing information for EXOC8 Gene Joubert syndrome EXOC8 related Genetic Test
Symptoms of EXOC8 Gene Joubert Syndrome Joubert syndrome is a rare genetic disorder that affects the development of the cerebellum, a part of the brain that controls balance and coordination. The EXOC8 gene has been identified as one of the genetic contributors to this condition. Symptoms of Joubert syndrome related to mutations in the EXOC8 […]
Symptoms and Testing information for CC2D2A Gene Joubert syndrome type 9 Genetic Test
Joubert Syndrome is a rare genetic disorder that affects the development of the cerebellum, an area of the brain that controls balance and coordination. Type 9 of this syndrome, specifically, is caused by mutations in the CC2D2A gene. Recognizing the symptoms early on can be crucial for the management and treatment of the condition. DNA […]
Symptoms and Testing information for ARL13B Gene Joubert Syndrome Type 8 Genetic Test
Symptoms of ARL13B Gene Joubert Syndrome Type 8 Joubert Syndrome is a rare genetic disorder that affects the cerebellum, an area of the brain that controls balance and coordination. Joubert Syndrome Type 8, specifically linked to mutations in the ARL13B gene, exhibits a range of clinical symptoms that can vary significantly from one individual to […]
Symptoms and Testing information for RPGRIP1L Gene Joubert Syndrome Type 7 Genetic Test
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services to help individuals and families understand their genetic makeup and potential health risks. One of the critical tests provided by DNA Labs UAE is for Joubert Syndrome Type 7, caused by mutations in the RPGRIP1L gene. This […]