Sale!

SBDS Gene Aplastic anemia SBDS related Genetic Test Cost

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

-21%

The SBDS gene plays a crucial role in the development and maintenance of the bone marrow, which is essential for producing healthy blood cells. Mutations in the SBDS gene can lead to a rare and serious condition known as Shwachman-Diamond Syndrome (SDS), which can manifest in various ways, including aplastic anemia. Aplastic anemia is a disorder where the bone marrow fails to produce sufficient amounts of blood cells, leading to a host of health issues including fatigue, higher risk of infections, and bleeding disorders.

To diagnose or confirm a link between SBDS gene mutations and aplastic anemia, a genetic test can be conducted. In the UAE, DNA Labs offers a specialized test for this purpose. This test involves analyzing the patient’s DNA to identify mutations in the SBDS gene that are associated with Shwachman-Diamond Syndrome and its related aplastic anemia.

The cost of the SBDS gene-related genetic test at DNA Labs UAE is 4400 AED. This test is crucial for individuals who exhibit symptoms of aplastic anemia or have a family history of SDS, as it can provide a definitive diagnosis. A positive result can guide the treatment plan and also offers the possibility of genetic counseling for affected families, helping them understand the risks and implications for future offspring.

It’s important to note that such a test should be conducted under the guidance of a healthcare professional or genetic counselor, who can interpret the results accurately and offer the appropriate advice and support.

Description

SBDS Gene Aplastic Anemia SBDS Related Genetic Test

Test Name: SBDS Gene Aplastic Anemia SBDS Related Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 SBDS Gene Aplastic Anemia, SBDS Related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Aplastic Anemia, SBDS Related.

Test Details:

Aplastic anemia is a rare and serious blood disorder characterized by a decrease in the production of red blood cells, white blood cells, and platelets in the bone marrow. It can be caused by a variety of factors, including genetic mutations. The SBDS gene is associated with a specific type of aplastic anemia called Shwachman-Diamond syndrome (SDS). Mutations in the SBDS gene are responsible for the majority of cases of SDS. SDS is a rare inherited disorder that affects various organs and systems in the body, including the bone marrow, pancreas, and skeletal system.

Next-generation sequencing (NGS) genetic testing is a technique used to analyze multiple genes simultaneously to identify mutations or variations that may be associated with a specific disease or condition. In the case of SBDS-related aplastic anemia, NGS genetic testing can be used to detect mutations in the SBDS gene that may be responsible for the development of the disease.

NGS genetic testing for SBDS-related aplastic anemia typically involves obtaining a blood or saliva sample from the individual undergoing testing. The sample is then sent to a laboratory where the DNA is extracted and sequenced using NGS technology. The sequencing data is then analyzed to identify any mutations or variations in the SBDS gene.

The results of the NGS genetic test can help confirm a diagnosis of SBDS-related aplastic anemia and provide valuable information for treatment and management of the condition. It can also help identify other family members who may be at risk of developing the disease.

It is important to note that NGS genetic testing is not a diagnostic tool on its own. The results of the test should be interpreted by a healthcare professional who specializes in genetics or genetic counseling. They can provide guidance on the implications of the test results and help with further management and treatment options.

Test Name	SBDS Gene Aplastic anemia SBDS related 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 SBDS Gene Aplastic anemia, SBDS related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Aplastic anemia, SBDS related
Test Details	Aplastic anemia is a rare and serious blood disorder characterized by a decrease in the production of red blood cells, white blood cells, and platelets in the bone marrow. It can be caused by a variety of factors, including genetic mutations. The SBDS gene is associated with a specific type of aplastic anemia called Shwachman-Diamond syndrome (SDS). Mutations in the SBDS gene are responsible for the majority of cases of SDS. SDS is a rare inherited disorder that affects various organs and systems in the body, including the bone marrow, pancreas, and skeletal system. Next-generation sequencing (NGS) genetic testing is a technique used to analyze multiple genes simultaneously to identify mutations or variations that may be associated with a specific disease or condition. In the case of SBDS-related aplastic anemia, NGS genetic testing can be used to detect mutations in the SBDS gene that may be responsible for the development of the disease. NGS genetic testing for SBDS-related aplastic anemia typically involves obtaining a blood or saliva sample from the individual undergoing testing. The sample is then sent to a laboratory where the DNA is extracted and sequenced using NGS technology. The sequencing data is then analyzed to identify any mutations or variations in the SBDS gene. The results of the NGS genetic test can help confirm a diagnosis of SBDS-related aplastic anemia and provide valuable information for treatment and management of the condition. It can also help identify other family members who may be at risk of developing the disease. It is important to note that NGS genetic testing is not a diagnostic tool on its own. The results of the test should be interpreted by a healthcare professional who specializes in genetics or genetic counseling. They can provide guidance on the implications of the test results and help with further management and treatment options.