BSND Gene Bartter Syndrome Type 4a Genetic Test
Components: BSND Gene Bartter syndrome type 4a 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: Hepatology Nephrology Endocrinology Disorders
Doctor: General Physician
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for BSND Gene Bartter syndrome type 4a NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BSND Gene Bartter syndrome type 4a NGS Genetic DNA Test gene BSND
Test Details:
The BSND gene encodes a protein called barttin, which is essential for the normal functioning of the kidneys and inner ear. Mutations in the BSND gene can cause a rare genetic disorder called Bartter syndrome type 4a. Bartter syndrome is a group of genetic disorders that affect the kidneys’ ability to reabsorb salt and maintain the body’s electrolyte balance. Individuals with Bartter syndrome often experience symptoms such as excessive urination, dehydration, salt cravings, muscle cramps, and growth problems.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. In the case of Bartter syndrome type 4a, NGS genetic testing can identify mutations in the BSND gene to confirm the diagnosis. This type of testing is highly accurate and can detect both common and rare genetic variations.
NGS genetic testing for Bartter syndrome type 4a involves obtaining a sample of the individual’s DNA, typically through a blood sample or saliva. The DNA is then sequenced using advanced technology, which can identify any mutations or variations in the BSND gene.
The results of the NGS genetic test can help healthcare providers determine the appropriate treatment and management strategies for individuals with Bartter syndrome type 4a. This may include medications to help regulate electrolyte levels, dietary changes, and regular monitoring of kidney function.
It is important to note that genetic testing for Bartter syndrome type 4a should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support.
| Test Name | BSND Gene Bartter syndrome type 4a 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 | Hepatology Nephrology Endocrinology Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for BSND Gene Bartter syndrome type 4a NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BSND Gene Bartter syndrome type 4a NGS Genetic DNA Test gene BSND |
| Test Details | The BSND gene encodes a protein called barttin, which is essential for the normal functioning of the kidneys and inner ear. Mutations in the BSND gene can cause a rare genetic disorder called Bartter syndrome type 4a. Bartter syndrome is a group of genetic disorders that affect the kidneys’ ability to reabsorb salt and maintain the body’s electrolyte balance. Individuals with Bartter syndrome often experience symptoms such as excessive urination, dehydration, salt cravings, muscle cramps, and growth problems. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously. In the case of Bartter syndrome type 4a, NGS genetic testing can identify mutations in the BSND gene to confirm the diagnosis. This type of testing is highly accurate and can detect both common and rare genetic variations. NGS genetic testing for Bartter syndrome type 4a involves obtaining a sample of the individual’s DNA, typically through a blood sample or saliva. The DNA is then sequenced using advanced technology, which can identify any mutations or variations in the BSND gene. The results of the NGS genetic test can help healthcare providers determine the appropriate treatment and management strategies for individuals with Bartter syndrome type 4a. This may include medications to help regulate electrolyte levels, dietary changes, and regular monitoring of kidney function. It is important to note that genetic testing for Bartter syndrome type 4a should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support. |
