CLCF1 Gene Cold-induced sweating syndrome type 2 Genetic Test
Welcome to DNA Labs UAE, where we offer the CLCF1 Gene Cold-induced sweating syndrome type 2 Genetic Test. This test is designed to diagnose and identify mutations in the CLCF1 gene that are responsible for Cold-induced sweating syndrome type 2 (CISS2), a rare genetic disorder characterized by abnormal sweating in response to cold temperatures.
Test Details
The CLCF1 Gene Cold-induced sweating syndrome type 2 Genetic Test is conducted using NGS (Next-Generation Sequencing) technology. NGS is an advanced sequencing method that allows us to analyze multiple genes simultaneously. In the case of CISS2, NGS is used to identify mutations in the CLCF1 gene.
Components and Price
The cost of the CLCF1 Gene Cold-induced sweating syndrome type 2 Genetic Test is AED 4400.0. The test can be performed using a blood sample, extracted DNA, or even just one drop of blood on an FTA card.
Report Delivery
After the test is conducted, the report will be delivered within 3 to 4 weeks.
Test Type and Department
The CLCF1 Gene Cold-induced sweating syndrome type 2 Genetic Test falls under the category of Dysmorphology and is performed in our Genetics department.
Doctor and Pre Test Information
For this test, we recommend consulting with a Pediatrics specialist. Before the test, it is important to provide the clinical history of the patient who is going for the CLCF1 Gene Cold-induced sweating syndrome type 2 NGS Genetic DNA Test. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected by the CLCF1 Gene Cold-induced sweating syndrome type 2 NGS Genetic DNA Test gene CLCF1.
Understanding CISS2 and the CLCF1 Gene
Cold-induced sweating syndrome type 2 (CISS2) is a rare genetic disorder that causes abnormal sweating in response to cold temperatures. It is caused by mutations in the CLCF1 gene. By conducting the NGS Genetic Test, we can identify these mutations and confirm a diagnosis of CISS2.
NGS Genetic Test Process
The NGS Genetic Test for CISS2 involves obtaining a DNA sample from the individual being tested. This can be done through a blood sample or a cheek swab. The DNA sample is then sequenced using NGS technology, which reads the genetic code of the CLCF1 gene and identifies any mutations present.
Benefits of the NGS Genetic Test
The results of the NGS Genetic Test can provide valuable information for genetic counseling, family planning, and potentially guide treatment options for individuals with CISS2. By understanding the specific mutations in the CLCF1 gene, healthcare professionals can offer personalized care and support to patients and their families.
| Test Name | CLCF1 Gene Cold-induced sweating syndrome type 2 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 CLCF1 Gene Cold-induced sweating syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CLCF1 Gene Cold-induced sweating syndrome type 2 NGS Genetic DNA Test gene CLCF1 |
| Test Details |
Cold-induced sweating syndrome type 2 (CISS2) is a rare genetic disorder characterized by abnormal sweating in response to cold temperatures. It is caused by mutations in the CLCF1 gene. NGS (Next-Generation Sequencing) Genetic Test is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of CISS2, NGS can be used to identify mutations in the CLCF1 gene that are responsible for the disorder. The NGS Genetic Test for CISS2 involves obtaining a DNA sample from the individual being tested, typically through a blood sample or cheek swab. The DNA is then sequenced using NGS technology, which reads the genetic code of the CLCF1 gene and identifies any mutations present. The results of the NGS Genetic Test can help confirm a diagnosis of CISS2 and provide information about the specific mutations in the CLCF1 gene. This information can be used for genetic counseling, family planning, and potentially guide treatment options for individuals with CISS2. |
