FGFR2 Gene Scaphocephaly Maxillary Retrusion and Mental Retardation Genetic Test
Welcome to DNA Labs UAE, where we offer comprehensive genetic testing services, including the FGFR2 gene test for scaphocephaly, maxillary retrusion, and mental retardation. Read on to learn more about this test and its benefits.
Test Name: FGFR2 Gene Scaphocephaly Maxillary Retrusion and Mental Retardation Genetic Test
Components:
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Method: NGS Technology
- Test Type: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information:
Prior to undergoing the FGFR2 gene test, it is important to provide the clinical history of the patient who is being tested for scaphocephaly, maxillary retrusion, and mental retardation. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by these conditions.
Test Details:
The FGFR2 gene is associated with various genetic disorders, including scaphocephaly, maxillary retrusion, and mental retardation. These conditions are typically diagnosed using Next Generation Sequencing (NGS) genetic testing.
Scaphocephaly is characterized by the premature fusion of the sagittal suture in the skull, resulting in an elongated and narrow head shape. Maxillary retrusion refers to the underdevelopment or recession of the upper jaw, leading to dental and facial abnormalities. Mental retardation, or intellectual disability, is characterized by significant limitations in intellectual functioning and adaptive behavior.
NGS genetic testing involves sequencing an individual’s DNA to identify any variations or mutations in specific genes, including the FGFR2 gene. This type of testing allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic abnormalities.
By identifying variations or mutations in the FGFR2 gene, NGS genetic testing can help confirm a diagnosis of scaphocephaly, maxillary retrusion, and mental retardation. This information is crucial in guiding treatment decisions, providing genetic counseling, and facilitating early intervention and management strategies.
At DNA Labs UAE, we understand the importance of accurate and timely genetic testing. Our experienced team of professionals utilizes state-of-the-art technology to deliver reliable results. Contact us today to schedule an appointment for the FGFR2 gene scaphocephaly, maxillary retrusion, and mental retardation genetic test.
Test Name | FGFR2 Gene Scaphocephaly maxillary retrusion and mental retardation Genetic Test |
---|---|
Components | |
Price | 4400.0 AED |
Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
Report Delivery | 3 to 4 Weeks |
Method | NGS Technology |
Test type | Dysmorphology |
Doctor | Pediatrics |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for FGFR2 Gene Scaphocephaly, maxillary retrusion, and mental retardation NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene Scaphocephaly, maxillary retrusion, and mental retardation NGS Genetic DNA Test gene FGFR2 |
Test Details |
The FGFR2 gene is associated with a number of genetic disorders, including scaphocephaly, maxillary retrusion, and mental retardation. These conditions are typically diagnosed using Next Generation Sequencing (NGS) genetic testing. Scaphocephaly is a condition characterized by the premature fusion of the sagittal suture in the skull, leading to an elongated and narrow head shape. Maxillary retrusion refers to the underdevelopment or recession of the upper jaw, which can result in dental and facial abnormalities. Mental retardation, also known as intellectual disability, is a condition characterized by significant limitations in intellectual functioning and adaptive behavior. NGS genetic testing involves sequencing the DNA of an individual to identify any variations or mutations in specific genes, including the FGFR2 gene. This type of testing allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic abnormalities. By identifying variations or mutations in the FGFR2 gene, NGS genetic testing can help confirm a diagnosis of scaphocephaly, maxillary retrusion, and mental retardation. This information can be valuable in guiding treatment decisions, providing genetic counseling, and facilitating early intervention and management strategies. |