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KRT6A Gene Pachyonychia Congenita Type 3 Genetic Test Cost

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

-21%

Pachyonychia Congenita Type 3, associated with mutations in the KRT6A gene, is a rare genetic disorder characterized by thickened nails, painful palmoplantar keratoderma, and other skin abnormalities. The condition stems from mutations in the KRT6A gene, which plays a crucial role in the production of keratin, a protein essential for the strength and integrity of skin, nails, and hair.

To diagnose this specific subtype of Pachyonychia Congenita, genetic testing is performed to identify mutations in the KRT6A gene. DNA Labs UAE offers a specialized genetic test for Pachyonychia Congenita Type 3, aimed at individuals who exhibit symptoms of the disorder or have a family history of the condition. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect mutations in the KRT6A gene.

The cost of the KRT6A Gene Pachyonychia Congenita Type 3 Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test is a crucial step in confirming the diagnosis, which can guide treatment options and help affected individuals and their families understand the implications of the disorder. Early diagnosis through genetic testing can also aid in the management of symptoms and improve the quality of life for those living with Pachyonychia Congenita Type 3.

Description

KRT6A Gene Pachyonychia congenita type 3 Genetic Test

Test Name: KRT6A Gene Pachyonychia congenita type 3 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 KRT6A Gene Pachyonychia congenita type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KRT6A Gene Pachyonychia congenita type 3 NGS Genetic DNA Test gene KRT6A

Test Details: The KRT6A gene is associated with Pachyonychia congenita type 3 (PC-3), which is a rare genetic disorder characterized by thickening of the nails and other skin abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the context of PC-3, NGS genetic testing can identify mutations or variants in the KRT6A gene that may be responsible for causing the disorder. This testing can help confirm a diagnosis, provide information about disease severity, and guide treatment options. During the NGS genetic testing process, a sample of DNA is collected, usually through a blood sample or saliva sample. The DNA is then sequenced, and the resulting data is analyzed to identify any mutations or variants in the KRT6A gene. The results are interpreted by genetic specialists who can provide information about the significance of any identified genetic changes. It is important to note that NGS genetic testing may not be available in all healthcare settings, and the specific genes analyzed may vary depending on the testing laboratory. Additionally, genetic testing for PC-3 may not be necessary in all cases, and the decision to pursue testing should be made in consultation with a healthcare professional or genetic counselor.

Test Name	KRT6A Gene Pachyonychia congenita type 3 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 KRT6A Gene Pachyonychia congenita type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KRT6A Gene Pachyonychia congenita type 3 NGS Genetic DNA Test gene KRT6A
Test Details	The KRT6A gene is associated with Pachyonychia congenita type 3 (PC-3), which is a rare genetic disorder characterized by thickening of the nails and other skin abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the context of PC-3, NGS genetic testing can identify mutations or variants in the KRT6A gene that may be responsible for causing the disorder. This testing can help confirm a diagnosis, provide information about disease severity, and guide treatment options. During the NGS genetic testing process, a sample of DNA is collected, usually through a blood sample or saliva sample. The DNA is then sequenced, and the resulting data is analyzed to identify any mutations or variants in the KRT6A gene. The results are interpreted by genetic specialists who can provide information about the significance of any identified genetic changes. It is important to note that NGS genetic testing may not be available in all healthcare settings, and the specific genes analyzed may vary depending on the testing laboratory. Additionally, genetic testing for PC-3 may not be necessary in all cases, and the decision to pursue testing should be made in consultation with a healthcare professional or genetic counselor.