Spag1 Gene Primary Ciliary Dyskinesia Type 28 NGS Genetic DNA Test
Introduction
The Spag1 Gene Primary Ciliary Dyskinesia Type 28 NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations associated with primary ciliary dyskinesia (PCD). PCD is a condition characterized by the dysfunction of cilia, which are tiny hair-like structures that play a crucial role in respiratory health. This test leverages Next Generation Sequencing (NGS) technology to provide precise genetic insights into this condition.
What the Test Measures
This test specifically measures variations in the Spag1 gene that are linked to PCD. By analyzing the genetic material, healthcare providers can determine if there are mutations that may contribute to the symptoms experienced by the patient.
Who Should Consider This Test?
Individuals who exhibit symptoms such as chronic respiratory infections, sinusitis, or unexplained fertility issues should consider this test. Risk factors include a family history of PCD or related disorders.
Benefits of Taking the Test
- Accurate diagnosis of primary ciliary dyskinesia.
- Informed treatment options based on genetic findings.
- Understanding of potential hereditary implications for family members.
- Access to specialized care from ENT doctors and geneticists.
Understanding Your Results
Results from the Spag1 Gene test will indicate whether any mutations were found. A genetic counseling session is recommended to discuss the implications of the findings and to assist in drawing a pedigree chart of family members affected by the condition.
Test Pricing
| Test Name | Discount Price (KSh) | Regular Price (KSh) |
|---|---|---|
| Spag1 Gene Primary Ciliary Dyskinesia Type 28 NGS Genetic DNA Test | 40,000 | 56,000 |
Branches and Booking
We have branches across all major cities in Kenya, providing convenient access to our testing services. Additionally, we offer home sample collection services for your convenience. Book your test today or contact us at +254711564616 for more information!
Additional Information
Turnaround Time: 3 to 4 weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, and a genetic counseling session should be arranged to discuss family history related to SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test.
