Micm Maternal Inherited Cardiomyopathy Mutation Detection Test
Introduction
The Micm Maternal Inherited Cardiomyopathy Mutation Detection Test is a groundbreaking diagnostic tool designed to identify genetic mutations associated with maternal inherited cardiomyopathy. This test plays a crucial role in early detection and management of heart diseases, allowing for timely interventions that can significantly improve patient outcomes.
What the Test Measures
This test detects specific genetic mutations linked to cardiomyopathy, a condition that affects the heart muscle and can lead to serious complications, including heart failure and arrhythmias. By analyzing the DNA from a blood sample, healthcare providers can determine if an individual has inherited mutations that increase their risk of developing this condition.
Who Should Consider This Test
Individuals with a family history of cardiomyopathy or related heart diseases should consider this test. Symptoms that may prompt testing include unexplained shortness of breath, fatigue, chest pain, or a family history of sudden cardiac death. Those at risk due to genetic predisposition can greatly benefit from early testing.
Benefits of Taking the Test
- Early diagnosis of potential heart diseases.
- Informed decision-making regarding lifestyle and treatment options.
- Peace of mind for individuals and families regarding genetic risks.
- Guidance for family planning and monitoring in at-risk individuals.
Understanding Your Results
Results from the Micm Maternal Inherited Cardiomyopathy Mutation Detection Test will indicate whether any genetic mutations have been detected. A positive result may suggest a higher risk of developing cardiomyopathy, prompting further evaluation and management by a cardiologist. It is essential to discuss the results with a healthcare provider to understand their implications fully.
Test Pricing
| Test Name | Discount Price (KSh) | Regular Price (KSh) |
|---|---|---|
| Micm Maternal Inherited Cardiomyopathy Mutation Detection Test | 21,000 | 21,840 |
Test Details
- Turnaround Time: Sample Daily by 11 am; Report in 10 days
- Sample Type: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
- Specialty: Cardiologist
- Department: Molecular Diagnostics
- Method: PCR
- Disease Type: Heart Diseases
Book Your Test Today!
We have branches across Kenya, making it easy for you to access our services. Don’t wait until it’s too late; take control of your heart health. Call or WhatsApp us at +254711564616 to book the Micm Maternal Inherited Cardiomyopathy Mutation Detection Test today!
