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ALOX12B Gene Ichthyosis congenital autosomal recessive type 2 Genetic Test Cost

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

-21%

The ALOX12B Gene Ichthyosis Congenital Autosomal Recessive Type 2 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the ALOX12B gene. These mutations are known to cause Autosomal Recessive Congenital Ichthyosis Type 2 (ARCI2), a rare genetic skin disorder characterized by severe scaling and thickening of the skin across the body. The 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 is crucial for early diagnosis and management of the condition, providing essential information for genetic counseling and understanding the risk of recurrence in families. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect the presence of specific mutations in the ALOX12B gene.

The cost of the ALOX12B Gene Ichthyosis Congenital Autosomal Recessive Type 2 Genetic Test at DNA Labs UAE is 4400 AED. This investment can be invaluable for families seeking answers to their loved one’s condition, allowing for a better understanding of the disease and facilitating informed decisions regarding care and treatment.

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ALOX12B Gene Ichthyosis congenital autosomal recessive type 2 Genetic Test

Test Name: ALOX12B Gene Ichthyosis congenital autosomal recessive type 2 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 ALOX12B Gene Ichthyosis, congenital, autosomal recessive, type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ALOX12B Gene Ichthyosis, congenital, autosomal recessive, type 2 NGS Genetic DNA Test gene ALOX12B.

Test Details

The ALOX12B gene is associated with a condition called ichthyosis, congenital, autosomal recessive, type 2. This is a genetic disorder characterized by dry, scaly skin (ichthyosis) that is present from birth (congenital) and is inherited in an autosomal recessive manner. 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 ALOX12B gene ichthyosis, NGS genetic testing can be used to identify any mutations or changes in the ALOX12B gene that may be responsible for the condition. This type of genetic testing can help in the diagnosis of ichthyosis and provide information about the specific genetic variants involved. It can also be useful for genetic counseling, determining the risk of passing on the condition to future generations, and guiding treatment options. It is important to consult with a healthcare professional or genetic counselor to discuss the specific details and implications of the ALOX12B gene ichthyosis NGS genetic test. They can provide personalized information and guidance based on an individual’s specific situation.

Test Name ALOX12B Gene Ichthyosis congenital autosomal recessive 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 ALOX12B Gene Ichthyosis, congenital, autosomal recessive, type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ALOX12B Gene Ichthyosis, congenital, autosomal recessive, type 2 NGS Genetic DNA Test gene ALOX12B
Test Details

The ALOX12B gene is associated with a condition called ichthyosis, congenital, autosomal recessive, type 2. This is a genetic disorder characterized by dry, scaly skin (ichthyosis) that is present from birth (congenital) and is inherited in an autosomal recessive manner.

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 ALOX12B gene ichthyosis, NGS genetic testing can be used to identify any mutations or changes in the ALOX12B gene that may be responsible for the condition.

This type of genetic testing can help in the diagnosis of ichthyosis and provide information about the specific genetic variants involved. It can also be useful for genetic counseling, determining the risk of passing on the condition to future generations, and guiding treatment options.

It is important to consult with a healthcare professional or genetic counselor to discuss the specific details and implications of the ALOX12B gene ichthyosis NGS genetic test. They can provide personalized information and guidance based on an individual’s specific situation.

SKU: TEST-3055 Category:

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