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CYP4F22 Gene Ichthyosis lamellar type 3 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 3,200 د.إ.

-43%

The “CYP4F22 Gene Ichthyosis Lamellar Type 3 Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the CYP4F22 gene, which are linked to the development of Lamellar Ichthyosis Type 3. Lamellar Ichthyosis is a rare genetic skin disorder characterized by the formation of large, dark, plate-like scales covering the body. This condition is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

The test aims to provide crucial genetic information that can assist in the early diagnosis and management of the condition. By identifying specific mutations in the CYP4F22 gene, healthcare providers can offer personalized treatment plans, genetic counseling, and support for affected individuals and their families. The genetic test is performed using a sample of the patient’s DNA, typically extracted from a blood sample.

At DNA Labs UAE, the cost of the CYP4F22 Gene Ichthyosis Lamellar Type 3 Genetic Test is set at 3200 AED. This investment in genetic testing can be invaluable for families seeking answers to their loved one’s condition, enabling them to make informed health and lifestyle decisions.

Description

CYP4F22 Gene Ichthyosis lamellar type 3 Genetic Test

Test Name: CYP4F22 Gene Ichthyosis lamellar type 3 Genetic Test

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

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 CYP4F22 Gene Ichthyosis, lamellar type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYP4F22 Gene Ichthyosis, lamellar type 3 NGS Genetic DNA Test gene CYP4F22

Test Details: CYP4F22 gene is associated with a specific type of ichthyosis called lamellar type 3. Ichthyosis is a group of genetic skin disorders characterized by dry, scaly skin. Lamellar type 3 is a rare form of ichthyosis that is caused by mutations in the CYP4F22 gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of CYP4F22 gene ichthyosis, NGS genetic testing can be used to identify mutations or variations in the CYP4F22 gene that may be causing the disease. The NGS genetic test for CYP4F22 gene ichthyosis involves collecting a sample of DNA, typically through a blood or saliva sample, from the affected individual. The DNA is then sequenced using NGS technology to analyze the CYP4F22 gene and identify any mutations or variations. This genetic test can help confirm a diagnosis of lamellar type 3 ichthyosis and provide information about the specific genetic cause of the condition. It can also be useful for genetic counseling and family planning purposes. It’s important to note that genetic testing for CYP4F22 gene ichthyosis should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations and support.

Test Name	CYP4F22 Gene Ichthyosis lamellar type 3 Genetic Test
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 CYP4F22 Gene Ichthyosis, lamellar type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CYP4F22 Gene Ichthyosis, lamellar type 3 NGS Genetic DNA Test gene CYP4F22
Test Details	CYP4F22 gene is associated with a specific type of ichthyosis called lamellar type 3. Ichthyosis is a group of genetic skin disorders characterized by dry, scaly skin. Lamellar type 3 is a rare form of ichthyosis that is caused by mutations in the CYP4F22 gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of CYP4F22 gene ichthyosis, NGS genetic testing can be used to identify mutations or variations in the CYP4F22 gene that may be causing the disease. The NGS genetic test for CYP4F22 gene ichthyosis involves collecting a sample of DNA, typically through a blood or saliva sample, from the affected individual. The DNA is then sequenced using NGS technology to analyze the CYP4F22 gene and identify any mutations or variations. This genetic test can help confirm a diagnosis of lamellar type 3 ichthyosis and provide information about the specific genetic cause of the condition. It can also be useful for genetic counseling and family planning purposes. It’s important to note that genetic testing for CYP4F22 gene ichthyosis should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations and support.