GGCX Gene Pseudoxanthoma Elasticum-like Disorder with Multiple Coagulation Factor Deficiency Genetic Test
Test Name: GGCX Gene Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Genetic Test
Components: GGCX gene pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency NGS genetic test
Price: 3200.0 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 GGCX Gene Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GGCX Gene Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency NGS Genetic DNA Test gene GGCX
Test Details: GGCX gene pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency NGS genetic test is a type of genetic test that is used to detect mutations in the GGCX gene. This gene is responsible for producing a protein called gamma-glutamyl carboxylase, which is involved in the activation of certain coagulation factors in the blood. Mutations in the GGCX gene can lead to a condition called pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency. This disorder is characterized by abnormal calcium deposits in the skin, eyes, and blood vessels, as well as a deficiency in certain coagulation factors, which can lead to an increased risk of bleeding. The NGS genetic test analyzes the DNA sequence of the GGCX gene to identify any mutations or variations that may be present. This can help in the diagnosis of pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency and can also be used for genetic counseling and family planning purposes. It is important to note that genetic testing should be done under the guidance of a healthcare professional, and the results should be interpreted in conjunction with a thorough clinical evaluation.
Test Name | GGCX Gene Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Genetic Test |
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Components | |
Price | 3200.0 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 GGCX Gene Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GGCX Gene Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency NGS Genetic DNA Test gene GGCX |
Test Details |
GGCX gene pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency NGS genetic test is a type of genetic test that is used to detect mutations in the GGCX gene. This gene is responsible for producing a protein called gamma-glutamyl carboxylase, which is involved in the activation of certain coagulation factors in the blood. Mutations in the GGCX gene can lead to a condition called pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency. This disorder is characterized by abnormal calcium deposits in the skin, eyes, and blood vessels, as well as a deficiency in certain coagulation factors, which can lead to an increased risk of bleeding. The NGS genetic test analyzes the DNA sequence of the GGCX gene to identify any mutations or variations that may be present. This can help in the diagnosis of pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency and can also be used for genetic counseling and family planning purposes. It is important to note that genetic testing should be done under the guidance of a healthcare professional, and the results should be interpreted in conjunction with a thorough clinical evaluation. |