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SATB2 Gene Glass Syndrome Genetic Test Cost

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

-21%

The SATB2 Gene Glass Syndrome Genetic Test is a specialized diagnostic procedure designed to identify mutations in the SATB2 gene, which are associated with Glass Syndrome. Glass Syndrome, also known as SATB2-associated syndrome (SAS), is a genetic condition characterized by developmental delays, intellectual disability, speech impairments, and distinctive facial features. The test involves analyzing the patient’s DNA to detect abnormalities in the SATB2 gene, providing crucial information for diagnosis, management, and genetic counseling.

Conducted at DNA Labs UAE, a leading facility in genetic testing, this test ensures accuracy and reliability in results. The cost of the SATB2 Gene Glass Syndrome Genetic Test is set at 4400 AED, reflecting the sophisticated technology and expertise involved in conducting the analysis. By opting for this test at DNA Labs UAE, individuals can gain insights into the genetic underpinnings of Glass Syndrome, facilitating informed decisions regarding treatment and care.

Description

SATB2 Gene Glass syndrome Genetic Test

Test Name: SATB2 Gene Glass syndrome 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: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for SATB2 Gene Glass syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SATB2 Gene Glass syndrome NGS Genetic DNA Test gene SATB2

Test Details: The SATB2 gene is responsible for producing a protein that plays a critical role in the development of the jaw, palate, and teeth. Mutations in this gene can lead to a rare genetic disorder known as SATB2-associated syndrome, also called Glass syndrome. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the identification of specific genetic variations or mutations that may be responsible for a particular disorder or condition. In the case of Glass syndrome, NGS genetic testing can be used to identify mutations in the SATB2 gene. This testing can help confirm a diagnosis of Glass syndrome in individuals who exhibit the characteristic symptoms of the disorder, such as intellectual disability, speech and language impairments, and dental abnormalities. NGS genetic testing may involve the sequencing of the entire SATB2 gene or specific regions of interest. The DNA sample required for testing can be obtained from a blood sample, saliva, or other tissues. By identifying the specific genetic mutation causing Glass syndrome, NGS genetic testing can provide valuable information for individuals and their families. It can help guide medical management and treatment options, provide accurate genetic counseling, and offer insights into the inheritance pattern of the disorder. It is important to note that NGS genetic testing for Glass syndrome is typically ordered by a healthcare professional with expertise in genetic disorders. The results of the test should be interpreted in conjunction with a thorough clinical evaluation to ensure accurate diagnosis and appropriate care.

Test Name	SATB2 Gene Glass 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 SATB2 Gene Glass syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SATB2 Gene Glass syndrome NGS Genetic DNA Test gene SATB2
Test Details	The SATB2 gene is responsible for producing a protein that plays a critical role in the development of the jaw, palate, and teeth. Mutations in this gene can lead to a rare genetic disorder known as SATB2-associated syndrome, also called Glass syndrome. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the identification of specific genetic variations or mutations that may be responsible for a particular disorder or condition. In the case of Glass syndrome, NGS genetic testing can be used to identify mutations in the SATB2 gene. This testing can help confirm a diagnosis of Glass syndrome in individuals who exhibit the characteristic symptoms of the disorder, such as intellectual disability, speech and language impairments, and dental abnormalities. NGS genetic testing may involve the sequencing of the entire SATB2 gene or specific regions of interest. The DNA sample required for testing can be obtained from a blood sample, saliva, or other tissues. By identifying the specific genetic mutation causing Glass syndrome, NGS genetic testing can provide valuable information for individuals and their families. It can help guide medical management and treatment options, provide accurate genetic counseling, and offer insights into the inheritance pattern of the disorder. It is important to note that NGS genetic testing for Glass syndrome is typically ordered by a healthcare professional with expertise in genetic disorders. The results of the test should be interpreted in conjunction with a thorough clinical evaluation to ensure accurate diagnosis and appropriate care.