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ASXL3 Gene Bainbridge-Ropers Syndrome Genetic Test Cost

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

-21%

The ASXL3 gene Bainbridge-Ropers Syndrome (BRPS) genetic test is a specialized diagnostic tool used to identify mutations in the ASXL3 gene, which are associated with Bainbridge-Ropers Syndrome. BRPS is a rare genetic disorder characterized by developmental delays, intellectual disability, difficulties with speech and language, and distinctive facial features. The condition is inherited in an autosomal dominant pattern, meaning a mutation in just one copy of the gene is sufficient to cause the disorder.

The test involves analyzing the patient’s DNA, extracted from a blood sample, to search for specific mutations in the ASXL3 gene that are known to cause the syndrome. This test is crucial for confirming a diagnosis of BRPS, which can help in the management and treatment of the condition. Early diagnosis can also guide decisions regarding educational and therapeutic interventions.

The ASXL3 gene Bainbridge-Ropers Syndrome genetic test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the expertise required to accurately interpret the results. By opting for this test at DNA Labs UAE, patients and their families can expect reliable results, comprehensive support, and guidance on the implications of the findings for the patient’s health and care.

Description

ASXL3 Gene Bainbridge-Ropers Syndrome Genetic Test

Test Name: ASXL3 Gene Bainbridge-Ropers Syndrome 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: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for ASXL3 Gene Bainbridge-Ropers Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ASXL3 Gene Bainbridge-Ropers Syndrome NGS Genetic DNA Test gene ASXL3

Test Details:

The ASXL3 gene is associated with a rare genetic disorder called Bainbridge-Ropers syndrome. This syndrome is characterized by developmental delay, intellectual disability, severe speech impairment, and distinct facial features.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Bainbridge-Ropers syndrome, NGS genetic testing can be used to identify mutations or variants in the ASXL3 gene that may be responsible for the disorder. By analyzing the entire coding region of the ASXL3 gene, NGS testing can provide a comprehensive assessment of any genetic abnormalities that may be present. This can help in confirming a diagnosis of Bainbridge-Ropers syndrome and provide valuable information for genetic counseling and management of the condition.

Test Name	ASXL3 Gene Bainbridge-Ropers syndrome 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	Dysmorphology
Doctor	Pediatrics
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for ASXL3 Gene Bainbridge-Ropers syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ASXL3 Gene Bainbridge-Ropers syndrome NGS Genetic DNA Test gene ASXL3
Test Details	The ASXL3 gene is associated with a rare genetic disorder called Bainbridge-Ropers syndrome. This syndrome is characterized by developmental delay, intellectual disability, severe speech impairment, and distinct facial features. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Bainbridge-Ropers syndrome, NGS genetic testing can be used to identify mutations or variants in the ASXL3 gene that may be responsible for the disorder. By analyzing the entire coding region of the ASXL3 gene, NGS testing can provide a comprehensive assessment of any genetic abnormalities that may be present. This can help in confirming a diagnosis of Bainbridge-Ropers syndrome and provide valuable information for genetic counseling and management of the condition.