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DBH Gene Dopamine beta-hydroxylase DBH deficiency Genetic Test Cost

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

-21%

The DBH Gene Dopamine beta-hydroxylase (DBH) deficiency genetic test is a specialized diagnostic tool used to detect abnormalities or mutations in the DBH gene, which can lead to dopamine beta-hydroxylase deficiency. This condition is rare and affects the body’s ability to produce norepinephrine and epinephrine from dopamine, leading to various autonomic nervous system dysfunctions. Symptoms can include orthostatic hypotension, ptosis, nasal congestion, and severe physical fatigue.

The test is performed by DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The procedure involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to identify any mutations in the DBH gene.

The cost of the DBH Gene Dopamine beta-hydroxylase (DBH) deficiency genetic test at DNA Labs UAE is 4400 AED. This cost covers the entire testing process, from sample collection to the analysis and reporting of results. It is important for patients considering this test to consult with a healthcare provider to understand the implications of the results and potential next steps in managing the condition if a mutation is detected.

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DBH Gene Dopamine beta-hydroxylase DBH deficiency Genetic Test

Test Name: DBH Gene Dopamine beta-hydroxylase DBH deficiency Genetic Test

Components: DBH gene analysis for mutations or variations

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: Cardiovascular Pneumology Disorders

Doctor: Cardiologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for DBH Gene Dopamine beta-hydroxylase (DBH) deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DBH Gene Dopamine beta-hydroxylase (DBH) deficiency NGS Genetic DNA Test gene DBH

Test Details

The DBH Gene Dopamine beta-hydroxylase (DBH) deficiency NGS Genetic Test is a genetic test that analyzes the DBH gene for mutations or variations that may cause DBH deficiency. DBH deficiency is a rare genetic disorder characterized by a lack of the enzyme dopamine beta-hydroxylase, which is responsible for converting dopamine to norepinephrine in the body.

This test utilizes next-generation sequencing (NGS) technology to analyze the entire DBH gene, allowing for the detection of various types of genetic changes, including small point mutations, insertions, deletions, and larger structural variations. By identifying these genetic changes, the test can provide a diagnosis for individuals suspected of having DBH deficiency.

The test typically involves collecting a DNA sample, usually through a blood sample or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any genetic variations in the DBH gene.

The DBH Gene Dopamine beta-hydroxylase (DBH) deficiency NGS Genetic Test can be helpful in confirming a diagnosis of DBH deficiency, which can aid in the management and treatment of affected individuals. It can also be used for carrier testing in individuals with a family history of DBH deficiency or for prenatal testing in couples at risk of having a child with the condition.

It is important to note that this test is typically performed by a specialized laboratory or genetic testing facility and should be ordered and interpreted by a healthcare professional with expertise in genetics. Genetic counseling may also be recommended before and after testing to help individuals understand the implications of the test results and make informed decisions.

Test Name DBH Gene Dopamine beta-hydroxylase DBH deficiency 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 Cardiovascular Pneumology Disorders
Doctor Cardiologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for DBH Gene Dopamine beta-hydroxylase (DBH) deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DBH Gene Dopamine beta-hydroxylase (DBH) deficiency NGS Genetic DNA Test gene DBH
Test Details

DBH Gene Dopamine beta-hydroxylase (DBH) deficiency NGS Genetic Test is a genetic test that analyzes the DBH gene for mutations or variations that may cause DBH deficiency. DBH deficiency is a rare genetic disorder characterized by a lack of the enzyme dopamine beta-hydroxylase, which is responsible for converting dopamine to norepinephrine in the body.

This test utilizes next-generation sequencing (NGS) technology to analyze the entire DBH gene, allowing for the detection of various types of genetic changes, including small point mutations, insertions, deletions, and larger structural variations. By identifying these genetic changes, the test can provide a diagnosis for individuals suspected of having DBH deficiency.

The test typically involves collecting a DNA sample, usually through a blood sample or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology, and the resulting data is analyzed to identify any genetic variations in the DBH gene.

The DBH Gene Dopamine beta-hydroxylase (DBH) deficiency NGS Genetic Test can be helpful in confirming a diagnosis of DBH deficiency, which can aid in the management and treatment of affected individuals. It can also be used for carrier testing in individuals with a family history of DBH deficiency or for prenatal testing in couples at risk of having a child with the condition.

It is important to note that this test is typically performed by a specialized laboratory or genetic testing facility and should be ordered and interpreted by a healthcare professional with expertise in genetics. Genetic counseling may also be recommended before and after testing to help individuals understand the implications of the test results and make informed decisions.

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