Sale!

LMNA Gene Hutchinson-Gilford Progeria Genetic Test Cost

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

-21%

The LMNA Gene Hutchinson-Gilford Progeria Genetic Test is a specialized diagnostic assessment performed to detect mutations in the LMNA gene, which are responsible for Hutchinson-Gilford Progeria Syndrome (HGPS). This rare genetic disorder is characterized by accelerated aging in children, leading to premature death usually due to heart disease. The test involves analyzing the patient’s DNA to identify specific mutations in the LMNA gene that cause the production of an abnormal protein known as progerin. This protein is the key factor behind the rapid aging process associated with the syndrome.

Conducted at DNA Labs UAE, this test is crucial for the early detection and management of Hutchinson-Gilford Progeria Syndrome. Early diagnosis can help in the management of symptoms and in some cases, may prolong the life expectancy of the affected individual. The cost of the test is 4400 AED, reflecting the specialized nature of the genetic analysis and the expertise required to accurately interpret the results. By identifying the presence of the LMNA gene mutation, this test provides essential information for families and healthcare providers, paving the way for potential treatment options and supportive care measures tailored to the unique needs of the patient.

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

LMNA Gene Hutchinson-Gilford Progeria Genetic Test

Genetic testing plays a crucial role in diagnosing and managing genetic disorders. One such disorder is Hutchinson-Gilford progeria syndrome (HGPS), a rare condition characterized by accelerated aging in children. DNA Labs UAE offers a comprehensive genetic test for the LMNA gene associated with HGPS.

Test Details

The LMNA gene is responsible for Hutchinson-Gilford progeria syndrome. To identify any mutations or variations in this gene, DNA Labs UAE utilizes Next-generation sequencing (NGS) technology. NGS allows for the rapid and efficient sequencing of large amounts of genetic material.

Test Components and Price

The LMNA Gene Hutchinson-Gilford progeria Genetic Test is priced at 4400.0 AED. The test requires a blood or extracted DNA sample, or even just one drop of blood on an FTA card.

Report Delivery

The report for the LMNA Gene Hutchinson-Gilford progeria Genetic Test is delivered within 3 to 4 weeks.

Test Method

The test utilizes NGS technology to analyze the LMNA gene for any mutations or variations associated with HGPS.

Test Type

The LMNA Gene Hutchinson-Gilford progeria Genetic Test falls under the category of Dysmorphology.

Referring Doctor and Test Department

The test is recommended by pediatricians and falls under the Genetics department at DNA Labs UAE.

Pre Test Information

Prior to the test, a clinical history of the patient is obtained. Additionally, a Genetic Counselling session is conducted to draw a pedigree chart of family members affected by HGPS.

Why is the Test Important?

Identifying specific mutations in the LMNA gene associated with HGPS is crucial for confirming a diagnosis and providing appropriate medical management and treatment options. Genetic testing can also be used for carrier screening in families with a history of HGPS or for prenatal testing in cases where there is a known family history of the condition.

It is important to note that genetic testing for HGPS should always be performed by a qualified geneticist or genetic counselor who can interpret the results and provide appropriate counseling and support.

Test Name LMNA Gene Hutchinson-Gilford progeria 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 LMNA Gene Hutchinson-Gilford progeria NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LMNA Gene Hutchinson-Gilford progeria NGS Genetic DNA Test gene LMNA
Test Details

The LMNA gene is associated with Hutchinson-Gilford progeria syndrome (HGPS), a rare genetic disorder characterized by accelerated aging in children.

Next-generation sequencing (NGS) is a high-throughput DNA sequencing technology that allows for the rapid and efficient sequencing of large amounts of genetic material. In the context of genetic testing for HGPS, NGS can be used to analyze the LMNA gene for any mutations or variations that may be responsible for the condition.

The NGS genetic test for LMNA gene mutations in Hutchinson-Gilford progeria involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual suspected of having HGPS. The DNA is then sequenced using NGS technology, allowing for the identification of any variations or mutations in the LMNA gene.

Identifying specific mutations in the LMNA gene associated with HGPS can help confirm a diagnosis and provide important information for medical management and treatment options. Additionally, genetic testing can also be used for carrier screening in families with a history of HGPS or for prenatal testing in cases where there is a known family history of the condition.

It’s important to note that genetic testing for HGPS should be performed by a qualified geneticist or genetic counselor who can interpret the results and provide appropriate counseling and support.