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SKI Gene Shprintzen-Goldberg Syndrome Genetic Test Cost

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

-21%

The SKI Gene Shprintzen-Goldberg Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the SKI gene associated with Shprintzen-Goldberg Syndrome (SGS). Shprintzen-Goldberg Syndrome is a rare genetic disorder characterized by craniofacial anomalies, skeletal malformations, and cardiovascular defects, among other symptoms. The test aims to provide conclusive genetic evidence of the syndrome, which can significantly aid in the accurate diagnosis and tailored management of the condition. Conducted in the advanced facilities of DNA Labs UAE, the test ensures high accuracy and reliability. The cost of the SKI Gene Shprintzen-Goldberg Syndrome Genetic Test is set at 4400 AED, reflecting the comprehensive nature of the analysis and the sophisticated technology employed. This test is crucial for families seeking answers to clinical symptoms suggestive of SGS, offering them a clear path towards understanding the genetic underpinnings of the syndrome and facilitating informed decisions regarding treatment and management.

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SKI Gene Shprintzen-Goldberg Syndrome Genetic Test

Test Name: SKI Gene Shprintzen-Goldberg 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 SKI Gene Shprintzen-Goldberg Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SKI Gene Shprintzen-Goldberg Syndrome NGS Genetic DNA Test gene SKI

Test Details

The SKI Gene Shprintzen-Goldberg Syndrome NGS genetic test is a type of genetic test that is used to identify mutations or variations in the SKI gene that are associated with Shprintzen-Goldberg Syndrome (SGS). SGS is a rare genetic disorder characterized by various physical and developmental abnormalities, including skeletal abnormalities, craniofacial features, cardiovascular defects, and intellectual disability.

Next-generation sequencing (NGS) technology is utilized in this genetic test to analyze the entire coding region of the SKI gene. NGS allows for the simultaneous analysis of multiple genes or the entire exome, which can provide a more comprehensive understanding of the genetic variations associated with SGS.

By identifying mutations or variations in the SKI gene, this test can help in confirming a diagnosis of SGS, providing genetic counseling to affected individuals and their families, and potentially guiding treatment decisions. It is typically performed by collecting a blood or saliva sample from the individual undergoing testing, which is then sent to a specialized laboratory for analysis.

The results of the genetic test can help healthcare professionals in managing and treating individuals with Shprintzen-Goldberg Syndrome.

Test Name SKI Gene Shprintzen-Goldberg 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 SKI Gene Shprintzen-Goldberg syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SKI Gene Shprintzen-Goldberg syndrome NGS Genetic DNA Test gene SKI
Test Details

The SKI gene Shprintzen-Goldberg syndrome NGS genetic test is a type of genetic test that is used to identify mutations or variations in the SKI gene that are associated with Shprintzen-Goldberg syndrome (SGS). SGS is a rare genetic disorder characterized by various physical and developmental abnormalities, including skeletal abnormalities, craniofacial features, cardiovascular defects, and intellectual disability.

Next-generation sequencing (NGS) technology is utilized in this genetic test to analyze the entire coding region of the SKI gene. NGS allows for the simultaneous analysis of multiple genes or the entire exome, which can provide a more comprehensive understanding of the genetic variations associated with SGS.

By identifying mutations or variations in the SKI gene, this test can help in confirming a diagnosis of SGS, providing genetic counseling to affected individuals and their families, and potentially guiding treatment decisions. It is typically performed by collecting a blood or saliva sample from the individual undergoing testing, which is then sent to a specialized laboratory for analysis. The results of the genetic test can help healthcare professionals in managing and treating individuals with Shprintzen-Goldberg syndrome.

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