NIPAL4 Gene Ichthyosiform Erythroderma Congenital Nonbullous Type 1 NGS Genetic DNA Test
Introduction
The NIPAL4 Gene Ichthyosiform Erythroderma Congenital Nonbullous Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool that assesses genetic predispositions to a rare skin condition known as ichthyosiform erythroderma. This test is crucial for individuals who have a family history of this disorder, allowing for early diagnosis and tailored management strategies.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to identify mutations in the NIPAL4 gene that are associated with congenital nonbullous ichthyosiform erythroderma. By analyzing the genetic code, healthcare providers can determine the likelihood of the disorder manifesting in patients or their offspring.
Who Should Consider This Test
Individuals with a family history of ichthyosiform erythroderma or those exhibiting symptoms such as severe skin dryness, scaling, and inflammation should consider this test. Risk factors include a genetic predisposition to dermatological disorders.
Benefits of Taking the Test
- Early diagnosis and intervention can significantly improve quality of life.
- Informs treatment options and management strategies tailored to the patient’s genetic profile.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the NIPAL4 Gene test will indicate whether any mutations are present. It is essential to consult with a genetic counselor or dermatologist to interpret these results accurately and understand the implications for health management.
Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| NIPAL4 Gene Ichthyosiform Erythroderma Congenital Nonbullous Type 1 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To take the first step towards understanding your genetic health, book the NIPAL4 Gene Ichthyosiform Erythroderma Congenital Nonbullous Type 1 NGS Genetic DNA Test today! For inquiries and appointments, please call or WhatsApp us at +2348077798758.
Turnaround time for results is approximately 3 to 4 weeks, and the sample type required can be blood or extracted DNA, or one drop of blood on an FTA card. Prior to the test, a clinical history consultation is necessary, along with a genetic counseling session to draw a pedigree chart of affected family members.
This test is conducted under the specialties of dermatology and genetics, focusing on osteology, dermatology, and immunology disorders.
