Symptoms and Testing information for NDE1 Gene Lissencephaly type 4 with microcephaly Genetic Test

Symptoms and Testing information for NDE1 Gene Lissencephaly type 4 with microcephaly Genetic Test

Lissencephaly, a rare, gene-linked brain formation disorder, presents significant challenges not only to the affected individuals but also to their families and healthcare providers. Among its various types, Lissencephaly type 4 with microcephaly, caused by mutations in the NDE1 gene, is particularly notable. Understanding the symptoms and the availability of genetic testing can be crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for this condition, priced at 4400 AED. For more information, visit DNA Labs UAE.

Symptoms of NDE1 Gene Lissencephaly Type 4 with Microcephaly

Lissencephaly type 4, associated with mutations in the NDE1 gene, manifests through a spectrum of neurological and physical symptoms. The hallmark of this disorder is microcephaly, a condition where the head circumference is significantly smaller than normal for the baby’s sex and gestational age. This is due to abnormal brain development characterized by “smooth brain” or reduced brain folds and grooves. The severity of symptoms can vary, but they generally include:

  • Severe intellectual disability
  • Developmental delays, including in motor skills and speech
  • Difficulty swallowing and feeding
  • Muscle stiffness or hypotonia (reduced muscle tone)
  • Seizures, which can be difficult to manage
  • Respiratory problems
  • Abnormalities in brain structure, visible through MRI or CT scans

Early detection and intervention are crucial for managing the symptoms of Lissencephaly type 4 and improving the quality of life for affected individuals. Genetic testing plays a pivotal role in this early diagnostic process.

Genetic Test for NDE1 Gene Lissencephaly Type 4 with Microcephaly

DNA Labs UAE offers a genetic test specifically designed to detect mutations in the NDE1 gene associated with Lissencephaly type 4 with microcephaly. The test, priced at 4400 AED, is a valuable tool for families seeking answers to developmental concerns in their children. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the lab for the presence of mutations in the NDE1 gene.

The benefits of undergoing this genetic test include:

  • Confirmation of the diagnosis, allowing for a more targeted approach to treatment and management
  • Information on the risk of recurrence in future pregnancies, which is crucial for family planning decisions
  • Access to support groups and resources for families affected by Lissencephaly
  • Potential eligibility for clinical trials or emerging therapies aimed at treating or managing the condition

While the cost of the test may seem high, the value it provides in terms of diagnostic clarity and subsequent management options can be immeasurable for affected families. Financial assistance programs may be available to help offset the cost for eligible families.

Conclusion

Lissencephaly type 4 with microcephaly is a challenging condition, but understanding its symptoms and the availability of genetic testing can empower families to seek early intervention and appropriate care. DNA Labs UAE’s genetic test for the NDE1 gene mutation offers hope for accurate diagnosis and the potential for better management of this rare disorder. For more details on the test and how to proceed, please visit DNA Labs UAE.

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