Symptoms of Paroxysmal Nocturnal Hemoglobinuria (PNH)
Paroxysmal Nocturnal Hemoglobinuria (PNH) is a rare, acquired, life-threatening disease of the blood characterized by the destruction of red blood cells, bone marrow failure, and blood clots. Understanding the symptoms of PNH is crucial for timely diagnosis and management of the condition. The most common symptoms include fatigue, difficulty in breathing, dark-colored urine (especially in the morning), anemia, blood clots, and frequent infections. Patients may also experience abdominal pain, headaches, and difficulty swallowing. The severity and combination of symptoms can vary widely among individuals, making PNH a challenging condition to diagnose based solely on clinical presentation.
Importance of Comprehensive Work-Up in PNH
The diagnosis of PNH requires a comprehensive work-up due to its complex nature and the variability of symptoms. Flow cytometry is the gold standard for diagnosing PNH, as it allows for the precise identification of PNH clones. This method involves analyzing the presence or absence of specific proteins on the surface of blood cells. The absence of these proteins indicates the presence of PNH clones, which are responsible for the symptoms of the disease.
Flow Cytometry: Flaer CD14 CD15 CD24 CD45CD59 CD64 GLY-A Test
The Flow Cytometry: Flaer CD14 CD15 CD24 CD45CD59 CD64 GLY-A Test is a comprehensive diagnostic test used to identify PNH clones in blood samples. This test examines the expression of several markers on the surface of white blood cells (CD14, CD15, CD24, CD64, and GLY-A) and red blood cells (FLAER, CD59, and CD55). The absence or reduced expression of these markers is indicative of PNH. This detailed analysis is essential for confirming the diagnosis of PNH and for determining the extent of the disease, which is critical for guiding treatment decisions.
Test Cost
The cost of the Flow Cytometry: Flaer CD14 CD15 CD24 CD45CD59 CD64 GLY-A Test is 2400 AED. While the cost may seem significant, it is important to consider the comprehensive nature of this test and its importance in accurately diagnosing PNH. Early and accurate diagnosis is crucial for managing PNH effectively and improving patient outcomes.
Why Choose DNA Labs UAE?
DNA Labs UAE is a leading provider of genetic testing services in the United Arab Emirates. With a state-of-the-art laboratory and a team of experienced professionals, DNA Labs UAE offers a wide range of genetic tests, including the comprehensive work-up for PNH. By choosing DNA Labs UAE for your diagnostic needs, you benefit from accurate and reliable results, timely reports, and exceptional customer service. For more information about the PNH Comprehensive Work-Up Flowcytometry-Flaer CD14 CD15 CD24 CD45CD59 CD64 GLY-A Test, please visit our website at DNA Labs UAE.
Conclusion
PNH is a rare but serious blood disorder that requires timely and accurate diagnosis for effective management. The Flow Cytometry: Flaer CD14 CD15 CD24 CD45CD59 CD64 GLY-A Test offered by DNA Labs UAE is an essential tool in diagnosing PNH, providing comprehensive analysis of blood cells to identify PNH clones. With the expertise of DNA Labs UAE and the detailed insights provided by this test, patients and healthcare providers can take informed steps towards managing PNH effectively. The investment in the test cost of 2400 AED is a valuable step towards securing accurate diagnosis and optimal care for individuals suspected of having PNH.
