POMC Gene Obesity early-onset susceptibility to 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:
Hepatology Nephrology Endocrinology Disorders
Doctor:
General Physician
Test Department:
Genetics
Pre Test Information:
Clinical History of Patient who is going for POMC Gene Obesity, early-onset, susceptibility to NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with POMC Gene Obesity, early-onset, susceptibility to NGS Genetic DNA Test gene POMC
Test Details:
The POMC gene is a gene that encodes a protein called pro-opiomelanocortin, which plays a crucial role in regulating appetite and energy balance in the body. Mutations in the POMC gene can lead to a rare genetic disorder known as POMC deficiency obesity, characterized by severe early-onset obesity, adrenal insufficiency, and red hair pigmentation.
NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and detect genetic variations or mutations associated with certain conditions. In the case of POMC gene obesity, an NGS genetic test can be performed to identify mutations in the POMC gene that may contribute to the development of obesity at an early age.
This genetic test involves sequencing the DNA of an individual, typically obtained through a blood or saliva sample. The DNA is then analyzed using NGS technology, which allows for the detection of variations in the POMC gene. These variations can include single nucleotide polymorphisms (SNPs), insertions, deletions, or other structural changes in the gene sequence.
By identifying specific mutations in the POMC gene, NGS genetic testing can help in diagnosing POMC deficiency obesity and determining the risk of developing obesity at an early age. This information can be useful for personalized treatment and management strategies for individuals with this genetic condition.
It is important to note that genetic testing for POMC gene obesity is typically recommended for individuals with a strong family history of early-onset obesity or other symptoms associated with POMC deficiency. A healthcare professional or genetic counselor can provide more information about the appropriateness and availability of NGS genetic testing for this condition.
| Test Name | POMC Gene Obesity early-onset susceptibility to 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 | Hepatology Nephrology Endocrinology Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for POMC Gene Obesity, early-onset, susceptibility to NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with POMC Gene Obesity, early-onset, susceptibility to NGS Genetic DNA Test gene POMC |
| Test Details | The POMC gene is a gene that encodes a protein called pro-opiomelanocortin, which plays a crucial role in regulating appetite and energy balance in the body. Mutations in the POMC gene can lead to a rare genetic disorder known as POMC deficiency obesity, characterized by severe early-onset obesity, adrenal insufficiency, and red hair pigmentation. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and detect genetic variations or mutations associated with certain conditions. In the case of POMC gene obesity, an NGS genetic test can be performed to identify mutations in the POMC gene that may contribute to the development of obesity at an early age. This genetic test involves sequencing the DNA of an individual, typically obtained through a blood or saliva sample. The DNA is then analyzed using NGS technology, which allows for the detection of variations in the POMC gene. These variations can include single nucleotide polymorphisms (SNPs), insertions, deletions, or other structural changes in the gene sequence. By identifying specific mutations in the POMC gene, NGS genetic testing can help in diagnosing POMC deficiency obesity and determining the risk of developing obesity at an early age. This information can be useful for personalized treatment and management strategies for individuals with this genetic condition. It is important to note that genetic testing for POMC gene obesity is typically recommended for individuals with a strong family history of early-onset obesity or other symptoms associated with POMC deficiency. A healthcare professional or genetic counselor can provide more information about the appropriateness and availability of NGS genetic testing for this condition. |
