ANKH Gene Chondrocalcinosis type 2 Genetic Test
Cost: AED 4400.0
Symptoms, Diagnosis, and Test Details
The ANKH gene is responsible for producing a protein called ANKH, which plays a role in the transport of inorganic pyrophosphate (PPi) out of cells. Mutations in the ANKH gene can lead to a condition called chondrocalcinosis type 2. Chondrocalcinosis type 2 is a rare genetic disorder characterized by the deposition of calcium pyrophosphate crystals in the joints, leading to joint pain, stiffness, and inflammation. It can also cause other skeletal abnormalities such as osteoarthritis and calcification of cartilage.
NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of chondrocalcinosis type 2, NGS genetic testing can be used to identify mutations in the ANKH gene that are associated with the condition. By identifying these mutations, NGS genetic testing can help confirm a diagnosis of chondrocalcinosis type 2 and provide information about the specific genetic variant involved. This information can be useful for genetic counseling, family planning, and potentially for guiding treatment decisions in the future.
Test Components and Price
- Test Name: ANKH Gene Chondrocalcinosis type 2 Genetic Test
- Price: AED 4400.0
Sample Condition
Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery
3 to 4 Weeks
Method
NGS Technology
Test Type
Osteology Dermatology Immunology Disorders
Doctor
Dermatologist
Test Department
Genetics
Pre Test Information
Clinical History of Patient who is going for ANKH Gene Chondrocalcinosis type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ANKH Gene Chondrocalcinosis type 2 NGS Genetic DNA Test gene ANKH
It’s important to note that genetic testing for chondrocalcinosis type 2 is typically done in a clinical setting and should be ordered and interpreted by a healthcare professional with expertise in genetics.
| Test Name | ANKH Gene Chondrocalcinosis 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 | Osteology Dermatology Immunology Disorders |
| Doctor | Dermatologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for ANKH Gene Chondrocalcinosis type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ANKH Gene Chondrocalcinosis type 2 NGS Genetic DNA Test gene ANKH |
| Test Details |
The ANKH gene is responsible for producing a protein called ANKH, which plays a role in the transport of inorganic pyrophosphate (PPi) out of cells. Mutations in the ANKH gene can lead to a condition called chondrocalcinosis type 2. Chondrocalcinosis type 2 is a rare genetic disorder characterized by the deposition of calcium pyrophosphate crystals in the joints, leading to joint pain, stiffness, and inflammation. It can also cause other skeletal abnormalities such as osteoarthritis and calcification of cartilage. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of chondrocalcinosis type 2, NGS genetic testing can be used to identify mutations in the ANKH gene that are associated with the condition. By identifying these mutations, NGS genetic testing can help confirm a diagnosis of chondrocalcinosis type 2 and provide information about the specific genetic variant involved. This information can be useful for genetic counseling, family planning, and potentially for guiding treatment decisions in the future. It’s important to note that genetic testing for chondrocalcinosis type 2 is typically done in a clinical setting and should be ordered and interpreted by a healthcare professional with expertise in genetics. |
