The HOXD13 Gene Syndactyly Type 1 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the HOXD13 gene, which are linked to Syndactyly Type 1. This condition is characterized by the fusion of two or more fingers or toes, and identifying genetic mutations can be crucial for accurate diagnosis, management, and understanding the risk of passing the condition to offspring. The test, priced at 4400 AED, involves analyzing the patient's DNA to detect abnormalities in the HOXD13 gene, providing valuable insights for patients and their families. DNA Labs UAE, known for its advanced genetic testing services, offers this test as part of its portfolio to assist in the early detection and intervention for genetic conditions like Syndactyly Type 1.
The HOXD13 Gene Syndactyly Type 5 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the HOXD13 gene, which are associated with Syndactyly Type 5. This condition is a congenital anomaly characterized by the fusion of certain fingers or toes, impacting the individual's hand or foot structure and function. The test is particularly crucial for families with a history of the condition, offering insights into genetic predispositions and aiding in early intervention strategies.
Conducted at DNA Labs UAE, a leading facility in genetic testing, this test employs advanced genetic sequencing technologies to accurately detect variations in the HOXD13 gene. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the specific gene mutations.
The cost of the HOXD13 Gene Syndactyly Type 5 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, covering the expenses of the sophisticated genetic analysis and the expertise required to interpret the results. Upon completion, the results provide valuable information that can guide clinical decisions, including surgical interventions or genetic counseling, thereby improving the quality of life for affected individuals and their families.
The BHLHA9 Gene Syndactyly Mesoaxial Synostotic with Phalangeal Reduction Genetic Test is a specialized diagnostic tool used to identify mutations in the BHLHA9 gene, which are associated with a rare genetic condition. This condition is characterized by the fusion of fingers or toes (syndactyly), specifically in a mesoaxial pattern, which affects the central digits. It also involves synostosis, where there is bone fusion leading to reduced mobility, and phalangeal reduction, where the phalanges (bones of the fingers and toes) are underdeveloped or missing.
This genetic test is crucial for early diagnosis and management of the condition, enabling healthcare providers to offer targeted treatments and interventions that can improve the quality of life for affected individuals. The test involves analyzing the patient's DNA to look for specific mutations in the BHLHA9 gene that are known to cause this complex syndactyly.
The test is offered by DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the expertise required to accurately interpret the results. For families and individuals facing the challenges of this rare condition, the BHLHA9 Gene Syndactyly Mesoaxial Synostotic with Phalangeal Reduction Genetic Test represents a vital step towards understanding their genetic makeup and accessing appropriate care and support.
The TANC2 gene plays a crucial role in brain development and function. Mutations or alterations in the TANC2 gene have been linked to various neurodevelopmental disorders, including intellectual disabilities, autism spectrum disorders, and other related conditions. To identify these genetic variations, a specific genetic test targeting the TANC2 gene can be performed.
This genetic test, available at DNA Labs UAE, is designed to detect mutations in the TANC2 gene that may be associated with brain-related disorders. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing it in the laboratory to identify any genetic abnormalities in the TANC2 gene.
The cost of the TANC2 Related Brain Disorders Genetic Test at DNA Labs UAE is 4400 AED. This price includes the collection of the sample, laboratory analysis, and a comprehensive report of the findings. The report not only indicates the presence of any genetic mutations in the TANC2 gene but also provides insights into the potential implications for the individual's neurological health and development. This information can be invaluable for early diagnosis, management, and intervention strategies for individuals and families affected by TANC2 related disorders.
The RBM10 Gene TARP Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the RBM10 gene, which are linked to TARP (Talipes equinovarus, Atrial septal defect, Robin sequence, and Persistent left superior vena cava) syndrome. TARP syndrome is a rare genetic condition that primarily affects males and can lead to a range of developmental issues and physical anomalies, including clubfoot, heart defects, difficulties in breathing and feeding, and distinctive facial features.
This test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to identify any genetic alterations in the RBM10 gene that might indicate the presence of TARP syndrome. The goal of the test is to provide accurate diagnosis, which can be crucial for early intervention, management of symptoms, and genetic counseling for affected families.
At DNA Labs UAE, the cost of the RBM10 Gene TARP Syndrome Genetic Test is set at 4400 AED. The test is conducted with high precision and confidentiality, ensuring that patients and their families receive comprehensive support and information regarding the condition and its implications.
The "Maternal UPD Chr. 14 Gene Temple Syndrome Genetic Test" is a specialized diagnostic tool available at DNA Labs UAE, designed to detect Temple Syndrome resulting from maternal uniparental disomy of chromosome 14 (UPD(14)mat). Temple Syndrome is a rare genetic disorder characterized by a range of symptoms including developmental delays, muscle weakness, feeding difficulties, and distinctive facial features. This condition is caused when a child inherits two copies of chromosome 14 from their mother and none from their father, leading to an imbalance in gene expression.
The test involves a comprehensive analysis of the genetic material to identify the specific chromosomal anomaly associated with Temple Syndrome. It is crucial for early diagnosis and management of the condition, allowing healthcare providers to offer targeted interventions and support to affected individuals and their families.
DNA Labs UAE offers this genetic test at a cost of 4400 AED. The lab is equipped with state-of-the-art technology and staffed by experienced professionals, ensuring accurate and reliable results. Families seeking answers about developmental concerns or individuals with a family history of Temple Syndrome may find this test particularly beneficial. It represents a crucial step towards understanding and managing the condition, offering hope and guidance for affected individuals.
The KCNH1 Gene Temple-Baraitser Syndrome Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the KCNH1 gene, which are linked to Temple-Baraitser Syndrome (TBS). TBS is a rare genetic disorder characterized by intellectual disability, epilepsy, distinct facial features, and abnormalities of the hands and feet. The test involves analyzing the patient's DNA to detect specific genetic alterations in the KCNH1 gene, providing crucial information for accurate diagnosis, management, and genetic counseling for affected families.
The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the KCNH1 gene. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test is a critical tool for healthcare providers in the diagnosis and treatment planning for individuals suspected of having Temple-Baraitser Syndrome. The result from this test not only aids in confirming the diagnosis but also helps in understanding the genetic basis of the condition, which can be vital for family planning and understanding the risk of recurrence in future pregnancies.
The CHSY1 gene Temtamy preaxial brachydactyly syndrome genetic test is a specialized diagnostic procedure available at DNA Labs UAE. This test specifically targets the CHSY1 gene, mutations in which are associated with Temtamy preaxial brachydactyly syndrome, a rare genetic disorder characterized by limb and digit abnormalities. The syndrome manifests through a spectrum of phenotypes, including shortened fingers and toes (brachydactyly), duplication of the thumb or big toe (preaxial polydactyly), and in some cases, additional skeletal anomalies.
The genetic test is crucial for accurate diagnosis, allowing for personalized medical management and genetic counseling for affected families. It involves the collection of a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the CHSY1 gene that are known to cause the syndrome.
The cost of the CHSY1 gene Temtamy preaxial brachydactyly syndrome genetic test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, covering the cost of the genetic analysis, the expertise of the laboratory personnel, and the detailed report provided to the patient or their healthcare provider. The report not only confirms the diagnosis but also offers insights into the condition's inheritance patterns, implications for family members, and possible interventions or management strategies.
Given the rarity of the condition and the specialized nature of the test, it represents a significant step forward in the field of genetic diagnostics in the UAE, offering hope and clarity to families affected by this challenging syndrome.
The C12orf57 gene Temtamy syndrome genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the C12orf57 gene, which are associated with Temtamy syndrome. Temtamy syndrome is a rare genetic disorder characterized by a spectrum of developmental anomalies including craniofacial abnormalities, intellectual disability, and other physical malformations. The test plays a crucial role in the early diagnosis and management of the syndrome, allowing for tailored care and intervention strategies.
Priced at 4400 AED, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for specific genetic mutations in the C12orf57 gene. The results can provide valuable information for affected individuals and their families regarding the prognosis, potential treatments, and the risk of passing the condition to future generations. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test is a vital tool for clinicians and genetic counselors in the diagnosis and understanding of Temtamy syndrome, ultimately facilitating better patient outcomes.
The WNT3 Gene Tetraamelia Autosomal Recessive Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the WNT3 gene, which are known to cause Tetraamelia Syndrome. This rare genetic disorder is characterized by the absence of all four limbs, along with other possible malformations involving the face, heart, nervous system, and genitals. The condition follows an autosomal recessive inheritance pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.
The test is crucial for families with a history of Tetraamelia Syndrome, as it helps in understanding the genetic risk of passing the condition to future generations. It is also valuable for affected individuals or carriers in terms of family planning and accessing appropriate genetic counseling services.
At DNA Labs UAE, the WNT3 Gene Tetraamelia Autosomal Recessive Genetic Test is offered at a cost of 4400 AED. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the WNT3 gene. The results can provide crucial information for diagnosis, treatment planning, and genetic counseling for affected families.
