Lactose primary intolerance – Genetic characterization – whole blood

Description

**Lactose Primary Intolerance – Genetic Characterization – Whole Blood**

**Introduction**
The Lactose Primary Intolerance – Genetic Characterization – Whole Blood test is a specialized diagnostic tool designed to identify genetic predispositions to lactose intolerance. By analyzing your DNA, this test provides a definitive answer to whether your body has the genetic markers associated with primary lactose intolerance, a condition that affects the ability to digest lactose, the sugar found in milk and dairy products. This test uses advanced molecular techniques to deliver accurate and reliable results, empowering you to make informed dietary and health decisions.

**Why You Need This Test**
Lactose intolerance is a common condition that can significantly impact your quality of life if left undiagnosed. This test is essential for individuals experiencing symptoms of lactose intolerance or those with a family history of the condition. Unlike temporary lactose intolerance caused by secondary factors, primary lactose intolerance is genetically determined. Identifying your genetic predisposition can help you understand your body’s ability to process lactose and guide you in managing your diet to avoid discomfort and long-term complications. This test is particularly valuable for individuals seeking a precise, science-backed diagnosis to differentiate between genetic and non-genetic causes of lactose intolerance.

**Symptoms That Indicate This Test**
You may need the Lactose Primary Intolerance – Genetic Characterization – Whole Blood test if you experience the following symptoms after consuming dairy products:
– Bloating or abdominal distension
– Diarrhea or loose stools
– Gas or excessive flatulence
– Stomach cramps or pain
– Nausea or vomiting
– Persistent discomfort after eating dairy

Additionally, this test is recommended for individuals with a family history of lactose intolerance or those who suspect they may have a genetic predisposition to the condition.

**Natural Production**
Lactose digestion depends on the enzyme lactase, which is produced in the small intestine. In individuals with primary lactose intolerance, the production of lactase decreases significantly after childhood due to genetic factors. This reduction in lactase activity leads to the inability to break down lactose into glucose and galactose, resulting in the symptoms of lactose intolerance. Genetic variations in the LCT gene, which regulates lactase production, are the primary cause of this condition. Understanding your genetic profile through this test can provide clarity on your body’s natural ability to process lactose.

**What Happens If Untreated**
Ignoring lactose intolerance can lead to chronic digestive discomfort and nutrient deficiencies. Persistent consumption of lactose-containing foods despite intolerance may cause inflammation, disrupt gut health, and lead to secondary complications such as irritable bowel syndrome (IBS). Additionally, avoiding dairy without proper diagnosis can result in calcium and vitamin D deficiencies, increasing the risk of osteoporosis and other bone-related conditions. Early diagnosis through this genetic test allows you to take proactive steps to manage your diet and prevent these long-term health risks.

**How to Prepare for the Test**
Preparation for the Lactose Primary Intolerance – Genetic Characterization – Whole Blood test is simple. No fasting or dietary restrictions are required. However, it is important to inform your healthcare provider about any medications or supplements you are taking, as these may affect the test results. Ensure you follow any specific instructions provided by your healthcare professional or the testing facility.

**Test Overview**
– **Sample Type**: EDTA whole blood
– **Methodology**: Kit LAMP Human Lactose Intolerance CE-IVD, Loop-mediated isothermal amplification
– **Turnaround Time (TAT)**: 37 days

This test uses cutting-edge molecular technology to analyze genetic markers associated with lactose intolerance. The process involves collecting a small blood sample, which is then analyzed in a certified laboratory. Results are typically available within 37 days, providing you with a comprehensive genetic profile related to lactose digestion.

**Call to Action**
Take control of your health and gain clarity on your body’s ability to process lactose with the Lactose Primary Intolerance – Genetic Characterization – Whole Blood test. Whether you’re experiencing symptoms or simply want to understand your genetic predisposition, this test offers accurate and actionable insights. Don’t let lactose intolerance disrupt your life—book your lab test today. Conveniently buy this diagnostic test online or find a diagnostic test near you to get started on your journey to better health.

**Category**: Molecular