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HOXB1 Gene Facial paresis type 3 Genetic Test Cost

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

-21%

The HOXB1 Gene Facial Paresis Type 3 Genetic Test is a specialized diagnostic tool used to identify mutations in the HOXB1 gene, which are associated with Facial Paresis Type 3, a rare genetic disorder. This condition is characterized by the partial or complete inability to move the muscles of the face, due to developmental issues affecting the facial nerves. The test is crucial for early detection and management of the disorder, allowing for appropriate interventions and support to be provided to affected individuals.

Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific genetic alterations in the HOXB1 gene. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic mutation responsible for the condition.

By opting for the HOXB1 Gene Facial Paresis Type 3 Genetic Test, individuals at risk or families with a history of the disorder can gain valuable insights into their genetic makeup, enabling informed healthcare decisions and personalized medical care to mitigate the effects of this challenging condition.

Description

HOXB1 Gene Facial Paresis Type 3 Genetic Test

Test Name: HOXB1 Gene Facial Paresis Type 3 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for HOXB1 Gene Facial Paresis Type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXB1 Gene Facial Paresis Type 3.

Test Details:

The HOXB1 gene is associated with facial paresis type 3, which is a condition characterized by weakness or paralysis of the facial muscles. This condition can affect facial expressions, speech, and eating.

NGS (next-generation sequencing) genetic testing can be used to identify mutations in the HOXB1 gene that may be causing facial paresis type 3. This type of testing can analyze multiple genes at once, providing a comprehensive view of an individual’s genetic makeup and potential risk for inherited conditions.

If a mutation is identified in the HOXB1 gene, genetic counseling and management strategies can be recommended to help manage symptoms and prevent complications.

Test Name	HOXB1 Gene Facial paresis type 3 Genetic Test
Components
Price	4400.0 AED
Sample Condition	Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery	3 to 4 Weeks
Method	NGS Technology
Test type	Neurological Disorders
Doctor	Neurologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for HOXB1 Gene Facial paresis type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HOXB1 Gene Facial paresis type 3
Test Details	The HOXB1 gene is associated with facial paresis type 3, which is a condition characterized by weakness or paralysis of the facial muscles. This condition can affect facial expressions, speech, and eating. NGS (next-generation sequencing) genetic testing can be used to identify mutations in the HOXB1 gene that may be causing facial paresis type 3. This type of testing can analyze multiple genes at once, providing a comprehensive view of an individual’s genetic makeup and potential risk for inherited conditions. If a mutation is identified in the HOXB1 gene, genetic counseling and management strategies can be recommended to help manage symptoms and prevent complications.