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HYLS1 Gene Hydrolethalus Syndrome Genetic Test Cost

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

-21%

The HYLS1 gene plays a critical role in human development, and mutations in this gene are associated with Hydrolethalus Syndrome (HLS), a rare genetic disorder characterized by severe malformations in the fetus, leading to prenatal or early postnatal death. Given the critical nature of early diagnosis for families with a history of HLS, the HYLS1 Gene Hydrolethalus Syndrome Genetic Test has become an essential tool in genetic counseling and prenatal care.

This genetic test specifically targets the HYLS1 gene to detect mutations that could lead to Hydrolethalus Syndrome. By analyzing the DNA, the test can provide vital information to expecting parents about the health of their fetus, enabling informed decisions during pregnancy. The test is particularly recommended for couples with a known family history of HLS or related symptoms, offering them a closer look at their baby’s genetic health.

Conducted at DNA Labs UAE, a leading facility in genetic testing, the HYLS1 Gene Test is performed with the utmost accuracy and confidentiality. The lab is equipped with state-of-the-art technology and staffed by professionals specialized in genetic diagnostics, ensuring high-quality results.

The cost of the HYLS1 Gene Hydrolethalus Syndrome Genetic Test is 4400 AED. While the price may seem significant, the value of the information it provides to at-risk families is immeasurable, potentially guiding critical healthcare decisions during pregnancy. It’s important for interested individuals to consult with their healthcare provider or a genetic counselor to understand the implications of the test results fully and to determine if this test is appropriate for their specific situation.

Description

HYLS1 Gene Hydrolethalus syndrome Genetic Test

Welcome to DNA Labs UAE, where we offer the HYLS1 Gene Hydrolethalus syndrome Genetic Test. This test is designed to diagnose individuals with Hydrolethalus syndrome and determine if they are carriers of the gene mutation. Below, you will find detailed information about the test, including its components, price, sample condition, report delivery, method, test type, doctor, test department, and pre-test information.

Test Details

The HYLS1 gene is associated with Hydrolethalus syndrome, a rare genetic disorder characterized by severe birth defects. This gene is responsible for the development and function of cilia, which are microscopic, finger-like projections on the surface of cells. Our NGS (Next-Generation Sequencing) genetic test analyzes the DNA sequence of the HYLS1 gene to identify any mutations or variations.

Components and Price

Test Name: HYLS1 Gene Hydrolethalus syndrome Genetic Test
Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on an FTA card for this test.

Report Delivery

You can expect to receive your test report within 3 to 4 weeks.

Method

We utilize NGS technology for this genetic test, which allows for rapid and efficient sequencing of large amounts of DNA.

Test Type

The test falls under the category of Dysmorphology.

Doctor

This test is conducted by our experienced pediatricians.

Test Department

Our Genetics department handles this specific test.

Pre Test Information

Prior to taking the HYLS1 Gene Hydrolethalus syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by HYLS1 Gene Hydrolethalus syndrome NGS Genetic DNA Test gene HYLS1.

By identifying mutations in the HYLS1 gene, NGS genetic testing can provide valuable information for genetic counseling, family planning, and potentially targeted treatments or interventions for individuals affected by Hydrolethalus syndrome.

For more information or to schedule an appointment for the HYLS1 Gene Hydrolethalus syndrome Genetic Test, please contact DNA Labs UAE.

Test Name	HYLS1 Gene Hydrolethalus 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 HYLS1 Gene Hydrolethalus syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HYLS1 Gene Hydrolethalus syndrome NGS Genetic DNA Test gene HYLS1
Test Details	The HYLS1 gene is a gene associated with Hydrolethalus syndrome, a rare genetic disorder characterized by severe birth defects. The HYLS1 gene provides instructions for making a protein that is involved in the development and function of cilia, which are microscopic, finger-like projections that stick out from the surface of cells. A NGS (Next-Generation Sequencing) genetic test for HYLS1 gene involves analyzing the DNA sequence of the gene to identify any mutations or variations that may be present. This test can help in diagnosing individuals with Hydrolethalus syndrome or determining if they are carriers of the gene mutation. NGS technology allows for the rapid and efficient sequencing of large amounts of DNA, making it a powerful tool for genetic testing. It can detect various types of genetic alterations, including single nucleotide variants (SNVs), insertions, deletions, and larger structural variations. By identifying mutations in the HYLS1 gene, NGS genetic testing can provide valuable information for genetic counseling, family planning, and potentially targeted treatments or interventions for individuals affected by Hydrolethalus syndrome.

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HYLS1 Gene Hydrolethalus Syndrome Genetic Test Cost

HYLS1 Gene Hydrolethalus syndrome Genetic Test