ESCO2 Gene Roberts Syndrome Genetic Test sale cost 4400 AED
PROP1 Gene Pituitary Hormone Deficiency Type 2 Genetic Test sale cost 4400 AED PROP1 Gene Pituitary Hormone Deficiency Type 2 Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
COL2A1 Gene SED Congenita Genetic Test sale cost 4400 AED COL2A1 Gene SED Congenita Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

ESCO2 Gene Roberts Syndrome Genetic Test Cost

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

-21%

The ESCO2 Gene Roberts Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the ESCO2 gene, which are responsible for Roberts Syndrome. This rare genetic disorder is characterized by growth delays, abnormalities in limb and facial development, and other systemic complications. By analyzing a patient’s DNA, the test can confirm a diagnosis of Roberts Syndrome, which is crucial for managing the condition and offering genetic counseling to families.

The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately detect the specific gene mutations. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test ensures reliability and confidentiality. Given the rarity of Roberts Syndrome, this genetic test plays a pivotal role in early detection and intervention, ultimately improving the quality of life for affected individuals.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

ESCO2 Gene Roberts Syndrome Genetic Test

Introduction

The ESCO2 gene Roberts syndrome NGS genetic test is a genetic test used to detect mutations or variations in the ESCO2 gene, which is associated with Roberts syndrome. Roberts syndrome is a rare genetic disorder characterized by limb and facial abnormalities, growth retardation, and intellectual disability.

Test Details

The ESCO2 gene Roberts syndrome NGS genetic test is conducted using Next-Generation Sequencing (NGS) technology. NGS is a high-throughput DNA sequencing technology that allows for the simultaneous sequencing of multiple genes or the entire genome. This technology enables the detection of various types of genetic variations, including single nucleotide variants, insertions, deletions, and structural rearrangements.

Components and Price

The test costs 4400.0 AED and requires a sample of either blood, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

The test results are typically delivered within 3 to 4 weeks.

Method

The ESCO2 gene Roberts syndrome NGS genetic test utilizes NGS technology for sequencing and analysis.

Test Type

The test falls under the category of Dysmorphology.

Doctor and Test Department

The test is performed by a Pediatrics doctor in the Genetics department.

Pre Test Information

A clinical history of the patient is required before undergoing the ESCO2 gene Roberts syndrome NGS genetic test. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by the ESCO2 gene mutation.

Test Purpose

The ESCO2 gene Roberts syndrome NGS genetic test helps confirm a diagnosis of Roberts syndrome in individuals with characteristic clinical features. It can also identify carriers of the ESCO2 gene mutation and be used for prenatal testing in families with a known ESCO2 gene mutation to determine the risk of having a child with Roberts syndrome.

Genetic Counseling

Genetic counseling is recommended before and after undergoing the ESCO2 gene Roberts syndrome NGS genetic test. This allows individuals and families to discuss the implications of the test results and receive support.

Test Name ESCO2 Gene Roberts 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 ESCO2 Gene Roberts syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ESCO2 Gene Roberts syndrome NGS Genetic DNA Test gene ESCO2
Test Details

ESCO2 gene Roberts syndrome NGS genetic test is a genetic test that is used to detect mutations or variations in the ESCO2 gene, which is associated with Roberts syndrome. Roberts syndrome is a rare genetic disorder characterized by limb and facial abnormalities, growth retardation, and intellectual disability.

NGS stands for Next-Generation Sequencing, which is a high-throughput DNA sequencing technology that allows for the simultaneous sequencing of multiple genes or the entire genome. This technology enables the detection of various types of genetic variations, including single nucleotide variants, insertions, deletions, and structural rearrangements.

The ESCO2 gene Roberts syndrome NGS genetic test involves collecting a sample of DNA, typically through a blood sample or buccal swab. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any mutations or variations in the ESCO2 gene.

The test can help confirm a diagnosis of Roberts syndrome in individuals with characteristic clinical features, as well as identify carriers of the ESCO2 gene mutation. It can also be used for prenatal testing in families with a known ESCO2 gene mutation to determine the risk of having a child with Roberts syndrome.

Genetic counseling is usually recommended before and after undergoing the ESCO2 gene Roberts syndrome NGS genetic test to discuss the implications of the test results and provide support to individuals and families.

SKU: TEST-4339 Category:

Related products