Symptoms and Testing information for ZFPM2 Gene Diaphragmatic hernia type 3 Genetic Test

Symptoms and Testing information for ZFPM2 Gene Diaphragmatic hernia type 3 Genetic Test

Diaphragmatic hernia is a serious condition that can affect newborns, leading to significant respiratory distress and requiring immediate medical attention. Among the genetic factors contributing to this condition, mutations in the ZFPM2 gene have been identified as a cause of Diaphragmatic Hernia Type 3. DNA Labs UAE offers a comprehensive genetic test specifically designed to identify mutations in the ZFPM2 gene, providing crucial information for expecting parents and medical professionals.

Symptoms of ZFPM2 Gene Diaphragmatic Hernia Type 3

Diaphragmatic Hernia Type 3, caused by mutations in the ZFPM2 gene, can lead to a range of symptoms, primarily affecting the respiratory system of newborns. The condition is characterized by a defect in the diaphragm, the muscle that separates the chest cavity from the abdominal cavity. This defect allows abdominal organs to move into the chest, compromising lung development and function. The most common symptoms include:

  • Severe respiratory distress shortly after birth
  • Blue discoloration of the skin due to lack of oxygen (cyanosis)
  • Rapid breathing (tachypnea)
  • Difficulty feeding
  • Poor growth
  • A barrel-shaped chest due to the displacement of abdominal organs into the thoracic cavity

It’s important to note that the severity of symptoms can vary significantly among affected individuals. In some cases, symptoms may be mild and not immediately life-threatening, while in others, they can lead to critical health issues requiring urgent medical intervention.

Importance of the ZFPM2 Gene Diaphragmatic Hernia Type 3 Genetic Test

Early detection of mutations in the ZFPM2 gene is crucial for the management and treatment of Diaphragmatic Hernia Type 3. The genetic test offered by DNA Labs UAE provides expectant parents with the opportunity to prepare for the necessary medical care and interventions that may be required after birth. For families with a history of diaphragmatic hernia, this test is particularly important as it can help assess the risk of recurrence in future pregnancies.

Test Procedure and Cost

The ZFPM2 Gene Diaphragmatic Hernia Type 3 Genetic Test involves a simple blood draw from the expectant mother. DNA extracted from the sample is then analyzed using advanced genetic sequencing techniques to identify any mutations in the ZFPM2 gene. The test is available at DNA Labs UAE for a cost of 4400 AED. While the price may seem high, the value of the information it provides cannot be overstated, especially for those with a family history of diaphragmatic hernias or other genetic conditions.

Conclusion

Diaphragmatic Hernia Type 3 is a serious condition that can have significant impacts on the health and development of newborns. Early detection through the ZFPM2 Gene Diaphragmatic Hernia Type 3 Genetic Test offered by DNA Labs UAE can provide families with crucial information for managing this condition. For more information on this test and to schedule an appointment, please visit DNA Labs UAE.

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