LHX3 Gene Pituitary Hormone Deficiency Combined Type 3 NGS Genetic DNA Test
Introduction
The LHX3 Gene Pituitary Hormone Deficiency Combined Type 3 NGS Genetic DNA Test is a specialized diagnostic tool designed to assess genetic variations associated with pituitary hormone deficiencies. This test utilizes Next Generation Sequencing (NGS) technology, providing a comprehensive analysis of the LHX3 gene, which plays a crucial role in endocrine function.
What the Test Measures
This test detects mutations in the LHX3 gene that may lead to combined pituitary hormone deficiencies. By identifying these genetic alterations, healthcare providers can better understand the underlying causes of hormonal imbalances and related disorders.
Who Should Consider This Test
This test is recommended for individuals experiencing symptoms such as:
- Growth delays in children
- Hormonal imbalances
- Hypopituitarism symptoms
- Family history of endocrine disorders
Risk factors include genetic predispositions and documented cases of pituitary disorders in family members.
Benefits of Taking the Test
- Accurate diagnosis of genetic conditions affecting hormone production.
- Guidance for personalized treatment plans.
- Insight into family health history and potential risks for future generations.
- Access to genetic counseling for better understanding of results and implications.
Understanding Your Results
Results from the LHX3 Gene Pituitary Hormone Deficiency Combined Type 3 NGS Genetic DNA Test will be interpreted by qualified geneticists. A comprehensive report will outline any detected mutations, their potential impact on health, and recommendations for management or further testing.
Test Details
| Test Name | Discount Price | Regular Price |
|---|---|---|
| LHX3 Gene Pituitary Hormone Deficiency Combined Type 3 NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card. Prior to the test, a clinical history of the patient is necessary, along with a genetic counseling session to create a pedigree chart of family members affected by LHX3 gene-related disorders.
We have branches across Kenya and offer home sample collection services for your convenience. To book your test or for more information, please call or WhatsApp us at +254746849631.
