FOXN1 Gene T-cell Immunodeficiency Congenital Alopecia and Nail Dystrophy Genetic Test
Are you concerned about T-cell immunodeficiency, congenital alopecia, and nail dystrophy? DNA Labs UAE offers the FOXN1 Gene T-cell immunodeficiency congenital alopecia and nail dystrophy genetic test to provide you with the answers you need.
Test Details
The FOXN1 gene is responsible for encoding a transcription factor that plays a crucial role in the development and function of T-cells, which are a type of white blood cell that plays a central role in the immune system. Mutations in the FOXN1 gene can lead to a condition known as T-cell immunodeficiency.
T-cell immunodeficiency is characterized by a weakened immune system, making individuals more susceptible to infections. This condition is typically present from birth (congenital) and can result in recurrent or severe infections, particularly those caused by viruses, fungi, and certain bacteria.
In addition to T-cell immunodeficiency, individuals with mutations in the FOXN1 gene may also present with congenital alopecia and nail dystrophy. Congenital alopecia refers to the absence or loss of hair at birth, while nail dystrophy refers to abnormalities in the growth and appearance of the nails.
Test Components and Price
The FOXN1 Gene T-cell immunodeficiency congenital alopecia and nail dystrophy genetic test is priced at 4400.0 AED. The test can be performed using blood or extracted DNA, or even just one drop of blood on an FTA card.
Report Delivery and Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes NGS (next-generation sequencing) technology, which allows for the simultaneous analysis of multiple genes, including the FOXN1 gene, to identify any mutations or variants that may be causing the condition.
Test Type and Doctor
The FOXN1 Gene T-cell immunodeficiency congenital alopecia and nail dystrophy genetic test falls under the category of Osteology Dermatology Immunology Disorders. It is recommended to consult with a dermatologist for this test.
Test Department and Pre-Test Information
The test is conducted by the Genetics department at DNA Labs UAE. Prior to the test, it is important to provide the clinical history of the patient who is going for the FOXN1 Gene T-cell immunodeficiency, congenital alopecia, and nail dystrophy NGS Genetic DNA Test. A Genetic Counselling session is also recommended to draw a pedigree chart of family members affected with the condition.
Importance of Genetic Testing
Genetic testing can help confirm the diagnosis, guide treatment decisions, and provide information on the inheritance pattern of the condition. It can also be useful for family planning purposes, as it can determine the risk of passing on the condition to future generations.
It is important to note that genetic testing should be carried out and interpreted by healthcare professionals with expertise in genetics, such as genetic counselors or medical geneticists, to ensure accurate diagnosis and appropriate management of the condition.
| Test Name | FOXN1 Gene T-cell immunodeficiency congenital alopecia and nail dystrophy 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 FOXN1 Gene T-cell immunodeficiency, congenital alopecia, and nail dystrophy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FOXN1 Gene T-cell immunodeficiency, congenital alopecia, and nail dystrophy NGS Genetic DNA Test gene FOXN1 |
| Test Details |
The FOXN1 gene is responsible for encoding a transcription factor that plays a crucial role in the development and function of T-cells, which are a type of white blood cell that plays a central role in the immune system. Mutations in the FOXN1 gene can lead to a condition known as T-cell immunodeficiency. T-cell immunodeficiency is characterized by a weakened immune system, making individuals more susceptible to infections. This condition is typically present from birth (congenital) and can result in recurrent or severe infections, particularly those caused by viruses, fungi, and certain bacteria. In addition to T-cell immunodeficiency, individuals with mutations in the FOXN1 gene may also present with congenital alopecia and nail dystrophy. Congenital alopecia refers to the absence or loss of hair at birth, while nail dystrophy refers to abnormalities in the growth and appearance of the nails. To diagnose FOXN1 gene-related T-cell immunodeficiency, congenital alopecia, and nail dystrophy, a next-generation sequencing (NGS) genetic test can be performed. NGS allows for the simultaneous analysis of multiple genes, including the FOXN1 gene, to identify any mutations or variants that may be causing the condition. Genetic testing can help confirm the diagnosis, guide treatment decisions, and provide information on the inheritance pattern of the condition. It can also be useful for family planning purposes, as it can determine the risk of passing on the condition to future generations. It is important to note that genetic testing should be carried out and interpreted by healthcare professionals with expertise in genetics, such as genetic counselors or medical geneticists, to ensure accurate diagnosis and appropriate management of the condition. |
