Sale!

NOTCH3 Mutation Detection CADASIL Test Cost

Original price was: 2,600 د.إ.Current price is: 2,340 د.إ.

-10%

The NOTCH3 Mutation Detection CADASIL Test is a specialized genetic test conducted to identify mutations in the NOTCH3 gene, which are associated with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL). CADASIL is a rare genetic disorder that leads to damage to the small blood vessels in the brain, contributing to a range of neurological symptoms such as migraines, cognitive decline, strokes, and mood disturbances. Early detection through the NOTCH3 Mutation Detection CADASIL Test can aid in the diagnosis and management of the condition, potentially improving the quality of life for affected individuals and their families.

The test is available at DNA Labs UAE, a reputable genetic testing facility known for its advanced diagnostic technologies and expert medical staff. The cost of the test is 2340 AED, making it a valuable investment for individuals with a family history of CADASIL or those exhibiting symptoms related to the disorder. By opting for this test at DNA Labs UAE, patients can expect accurate, reliable results and comprehensive support throughout the testing process, enabling informed healthcare decisions and personalized management strategies for CADASIL.

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

NOTCH3 MUTATION DETECTION CADASIL Test

Welcome to DNA Labs UAE, where we offer the NOTCH3 MUTATION DETECTION CADASIL Test. This genetic test is designed to detect mutations in the NOTCH3 gene, which is associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Test Details

The NOTCH3 mutation detection CADASIL test is used to identify any mutations or changes in the NOTCH3 gene. This test is typically ordered by a healthcare professional, such as a neurologist or geneticist, who specializes in diagnosing and managing CADASIL.

Components

  • NOTCH3 Gene

Price

The cost of the NOTCH3 MUTATION DETECTION CADASIL Test is 2340.0 AED.

Sample Condition

4 mL (2 mL min.) whole blood from 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Report Delivery

Sample collected on Monday by 11 am will have the report delivered on Friday.

Method

The NOTCH3 MUTATION DETECTION CADASIL Test is performed using PCR (Polymerase Chain Reaction) and sequencing techniques.

Test Type

This test falls under the category of Neurologic Disorder.

Doctor

This test is typically ordered by a Neurologist.

Test Department

This test is conducted in the Molecular Diagnostics department.

Pre Test Information

A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory prior to the test.

About CADASIL

CADASIL is a hereditary condition that affects the small blood vessels in the brain. It can lead to recurrent strokes, cognitive decline, and other neurological symptoms.

Importance of NOTCH3 Mutation Detection

Detecting a NOTCH3 mutation is crucial for both diagnostic and genetic counseling purposes. It allows individuals with CADASIL to receive appropriate medical management and treatment. Additionally, it helps identify at-risk family members who may benefit from genetic testing or counseling.

It’s important to note that the test results should be interpreted in conjunction with the individual’s clinical symptoms and family history.

Test Name NOTCH3 MUTATION DETECTION CADASIL Test
Components *NOTCH3 Gene
Price 2340.0 AED
Sample Condition 4 mL (2 mL min.) whole blood from 1 Lavender Top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery Sample Mon by 11 am; Report Fri
Method PCR, Sequencing
Test type Neurologic Disorder
Doctor Neurologist
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Details

The NOTCH3 mutation detection CADASIL test is a genetic test used to detect mutations in the NOTCH3 gene, which is associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). CADASIL is a hereditary condition that affects the small blood vessels in the brain, leading to recurrent strokes, cognitive decline, and other neurological symptoms.

The test involves analyzing a person’s DNA sample, typically obtained through a blood sample, to identify any mutations or changes in the NOTCH3 gene. This can help confirm a diagnosis of CADASIL and provide information about the specific genetic variant present.

Detection of a NOTCH3 mutation can be important for both diagnostic and genetic counseling purposes. It allows individuals with CADASIL to receive appropriate medical management and treatment, as well as helps identify at-risk family members who may benefit from genetic testing or counseling.

It’s important to note that this test is typically ordered by a healthcare professional, such as a neurologist or geneticist, who specializes in diagnosing and managing CADASIL. The test results should be interpreted in conjunction with the individual’s clinical symptoms and family history.