CHD7 Gene Kallmann Syndrome Type 5 Genetic Test sale cost 4400 AED
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CHD7 Gene Kallmann Syndrome Type 5 Genetic Test Cost

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

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The CHD7 gene Kallmann Syndrome Type 5 genetic test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the CHD7 gene, which are linked to the development of Kallmann Syndrome Type 5. This condition is a form of congenital hypogonadotropic hypogonadism, characterized by a lack of sense of smell (anosmia) and delayed or absent puberty, among other possible features such as hearing loss and renal anomalies. The test is critical for individuals showing symptoms of the syndrome or those with a family history of the condition, as it provides essential information for accurate diagnosis and management.

The testing process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect mutations in the CHD7 gene. A positive result indicates a mutation in the CHD7 gene that is known to cause Kallmann Syndrome Type 5, while a negative result can help rule out this specific genetic cause of the patient’s symptoms.

The cost of the CHD7 gene Kallmann Syndrome Type 5 genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to identify the genetic mutation, providing a crucial step towards a proper diagnosis and the development of an appropriate treatment plan for affected individuals. Given the specialized nature of this test and its significance in the management of Kallmann Syndrome Type 5, it represents a valuable tool in the field of genetic diagnostics.

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CHD7 Gene Kallmann syndrome type 5 Genetic Test

Components: CHD7 Gene Kallmann syndrome type 5 Genetic Test

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 CHD7 Gene Kallmann syndrome type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CHD7 Gene Kallmann syndrome type 5 NGS Genetic DNA Test gene CHD7

Test Details

The CHD7 gene is associated with a genetic disorder called Kallmann syndrome type 5. Kallmann syndrome is a rare genetic disorder that affects the development of the reproductive system and the sense of smell.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the case of Kallmann syndrome type 5, NGS genetic testing can identify mutations or variations in the CHD7 gene that may be responsible for the condition.

By analyzing the CHD7 gene using NGS technology, healthcare professionals can identify individuals who have Kallmann syndrome type 5 and provide appropriate medical management and genetic counseling. This type of genetic testing can also be used for carrier screening in families with a history of Kallmann syndrome type 5, helping individuals make informed decisions about family planning.

It is important to note that NGS genetic testing for Kallmann syndrome type 5 should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

Test Name CHD7 Gene Kallmann syndrome type 5 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 CHD7 Gene Kallmann syndrome type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CHD7 Gene Kallmann syndrome type 5 NGS Genetic DNA Test gene CHD7
Test Details

The CHD7 gene is associated with a genetic disorder called Kallmann syndrome type 5. Kallmann syndrome is a rare genetic disorder that affects the development of the reproductive system and the sense of smell.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the case of Kallmann syndrome type 5, NGS genetic testing can identify mutations or variations in the CHD7 gene that may be responsible for the condition.

By analyzing the CHD7 gene using NGS technology, healthcare professionals can identify individuals who have Kallmann syndrome type 5 and provide appropriate medical management and genetic counseling. This type of genetic testing can also be used for carrier screening in families with a history of Kallmann syndrome type 5, helping individuals make informed decisions about family planning.

It is important to note that NGS genetic testing for Kallmann syndrome type 5 should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

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