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BSND Gene Bartter Syndrome Type 4a Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The BSND Gene Bartter Syndrome Type 4a Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the BSND gene, which are associated with Bartter Syndrome Type 4a. This condition is a rare inherited disorder affecting the kidneys’ ability to reabsorb salt, leading to imbalances in electrolytes and various health complications such as dehydration, frequent urination, and growth retardation. The test plays a critical role in the early identification and management of the syndrome, providing essential information for personalized treatment plans. 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 the presence of genetic mutations in the BSND gene. Early diagnosis through the BSND Gene Bartter Syndrome Type 4a Genetic Test at DNA Labs UAE can significantly improve the quality of life for individuals with this condition by enabling timely interventions and appropriate care strategies.

Description

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.