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CASP8 Gene Autoimmune Lymphoproliferative Syndrome Type 2B Genetic Test Cost

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

-21%

The CASP8 Gene Autoimmune Lymphoproliferative Syndrome Type 2B Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the CASP8 gene, which are linked to Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS Type 2B). This rare genetic disorder is characterized by an abnormal immune system response that leads to the excessive production of lymphocytes, causing lymphadenopathy, splenomegaly, and an increased risk of autoimmune disorders and certain types of cancer. The test, priced at 4400 AED, is crucial for individuals suspected of having ALPS Type 2B, as it provides essential genetic insights that can guide treatment options, inform family planning decisions, and help manage the disease more effectively. DNA Labs UAE utilizes advanced genetic testing technologies to ensure accurate and reliable results for patients and their families.

Description

CASP8 Gene Autoimmune Lymphoproliferative Syndrome Type 2B Genetic Test

Test Name: CASP8 Gene Autoimmune Lymphoproliferative Syndrome Type 2B Genetic Test

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

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: Osteology Dermatology Immunology Disorders

Doctor: Dermatologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for CASP8 Gene Autoimmune Lymphoproliferative Syndrome Type 2B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CASP8 Gene Autoimmune Lymphoproliferative Syndrome Type 2B NGS Genetic DNA Test gene CASP8

Test Details: The CASP8 gene is a gene that encodes for the caspase-8 protein, which plays a crucial role in programmed cell death (apoptosis). Mutations in the CASP8 gene can lead to a rare genetic disorder called autoimmune lymphoproliferative syndrome type 2B (ALPS2B). ALPS2B is characterized by abnormal immune system function, leading to the accumulation of lymphocytes (a type of white blood cell) in various organs such as the lymph nodes, liver, and spleen. This can result in symptoms such as enlarged lymph nodes, hepatosplenomegaly (enlarged liver and spleen), autoimmune disorders, and an increased risk of developing certain types of cancer. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of ALPS2B, NGS genetic testing can be used to identify mutations in the CASP8 gene that may be responsible for the development of the disorder. By identifying these mutations, NGS genetic testing can help confirm a diagnosis of ALPS2B and provide important information for the management and treatment of the condition. It can also be used for genetic counseling and to assess the risk of passing on the condition to future generations.

Test Name	CASP8 Gene Autoimmune lymphoproliferative syndrome type 2B 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	Osteology Dermatology Immunology Disorders
Doctor	Dermatologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for CASP8 Gene Autoimmune lymphoproliferative syndrome type 2B NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CASP8 Gene Autoimmune lymphoproliferative syndrome type 2B NGS Genetic DNA Test gene CASP8
Test Details	The CASP8 gene is a gene that encodes for the caspase-8 protein, which plays a crucial role in programmed cell death (apoptosis). Mutations in the CASP8 gene can lead to a rare genetic disorder called autoimmune lymphoproliferative syndrome type 2B (ALPS2B). ALPS2B is characterized by abnormal immune system function, leading to the accumulation of lymphocytes (a type of white blood cell) in various organs such as the lymph nodes, liver, and spleen. This can result in symptoms such as enlarged lymph nodes, hepatosplenomegaly (enlarged liver and spleen), autoimmune disorders, and an increased risk of developing certain types of cancer. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of ALPS2B, NGS genetic testing can be used to identify mutations in the CASP8 gene that may be responsible for the development of the disorder. By identifying these mutations, NGS genetic testing can help confirm a diagnosis of ALPS2B and provide important information for the management and treatment of the condition. It can also be used for genetic counseling and to assess the risk of passing on the condition to future generations.