GLIS3 Gene Diabetes Mellitus Neonatal Genetic Test
Components
- Test Name: GLIS3 Gene Diabetes Mellitus Neonatal Genetic Test
- 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: Metabolic Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information
Clinical History of Patient who is going for GLIS3 Gene Diabetes Mellitus, Neonatal NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Diabetes Mellitus, Neonatal.
Test Details
The GLIS3 gene is associated with a form of diabetes called neonatal diabetes mellitus (NDM). NDM is a rare condition that is characterized by high blood sugar levels starting in the first few months of life. It is different from type 1 and type 2 diabetes, which typically develop later in childhood or adulthood.
A genetic test using next-generation sequencing (NGS) can help identify mutations or variations in the GLIS3 gene that may be causing NDM. NGS is a powerful technique that allows for the rapid sequencing of large amounts of DNA, making it an effective tool for identifying genetic causes of diseases. By analyzing the GLIS3 gene using NGS, healthcare providers can determine if there are any mutations or variations that are associated with NDM. This information can be helpful in diagnosing the condition and understanding its genetic basis.
Genetic testing for GLIS3 gene mutations may also be important for family planning purposes. If a parent carries a mutation in the GLIS3 gene, there is a chance that they could pass it on to their children, potentially resulting in NDM.
It is important to note that while genetic testing can provide valuable information, it is typically used in conjunction with other clinical evaluations and tests to make a definitive diagnosis. Additionally, genetic testing may not be available or recommended for all individuals with NDM, as it depends on the specific circumstances and clinical presentation of the patient.
If you or someone you know is concerned about NDM or the GLIS3 gene, it is recommended to consult with a healthcare professional or a genetic counselor who can provide personalized guidance and support.
| Test Name | GLIS3 Gene Diabetes mellitus neonatal 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for GLIS3 Gene Diabetes mellitus, neonatal NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Diabetes mellitus, neonatal |
| Test Details |
The GLIS3 gene is associated with a form of diabetes called neonatal diabetes mellitus (NDM). NDM is a rare condition that is characterized by high blood sugar levels starting in the first few months of life. It is different from type 1 and type 2 diabetes, which typically develop later in childhood or adulthood. A genetic test using next-generation sequencing (NGS) can help identify mutations or variations in the GLIS3 gene that may be causing NDM. NGS is a powerful technique that allows for the rapid sequencing of large amounts of DNA, making it an effective tool for identifying genetic causes of diseases. By analyzing the GLIS3 gene using NGS, healthcare providers can determine if there are any mutations or variations that are associated with NDM. This information can be helpful in diagnosing the condition and understanding its genetic basis. Genetic testing for GLIS3 gene mutations may also be important for family planning purposes. If a parent carries a mutation in the GLIS3 gene, there is a chance that they could pass it on to their children, potentially resulting in NDM. It is important to note that while genetic testing can provide valuable information, it is typically used in conjunction with other clinical evaluations and tests to make a definitive diagnosis. Additionally, genetic testing may not be available or recommended for all individuals with NDM, as it depends on the specific circumstances and clinical presentation of the patient. If you or someone you know is concerned about NDM or the GLIS3 gene, it is recommended to consult with a healthcare professional or a genetic counselor who can provide personalized guidance and support. |
