Symptoms and Testing information for ALX4 Gene Frontonasal Dysplasia Type 2 Genetic Test

Symptoms and Testing information for ALX4 Gene Frontonasal Dysplasia Type 2 Genetic Test

Frontonasal dysplasia type 2, caused by mutations in the ALX4 gene, is a rare genetic disorder. This condition is characterized by a range of physical malformations affecting the head and face, most notably the forehead and nose. Understanding the symptoms and undergoing genetic testing can be crucial for diagnosis, management, and family planning. DNA Labs UAE offers a comprehensive genetic test for this condition, priced at 4400 AED.

The ALX4 gene plays a critical role in the development of the craniofacial structure during embryonic growth. Mutations in this gene can disrupt normal development, leading to the manifestations of frontonasal dysplasia type 2. The symptoms can vary significantly in severity and presentation among affected individuals, but commonly include:

  • A widened space between the eyes (hypertelorism)
  • A broad nose with a split tip or notched appearance
  • A median cleft or groove of the nose and/or upper lip
  • A widow’s peak hairline
  • Craniosynostosis, where one or more of the sutures in the skull close prematurely
  • Underdevelopment or absence of the corpus callosum, affecting brain structure and function

Early diagnosis is crucial for managing the symptoms of frontonasal dysplasia type 2 and providing appropriate care and interventions. Genetic testing is the most reliable method for confirming a diagnosis, as it can identify mutations in the ALX4 gene that cause the disorder. The test offered by DNA Labs UAE involves collecting a DNA sample through a simple, non-invasive procedure. The sample is then analyzed in their state-of-the-art laboratory to detect any mutations in the ALX4 gene.

The cost of the ALX4 gene frontonasal dysplasia type 2 genetic test at DNA Labs UAE is 4400 AED. This price includes the collection of the DNA sample, analysis, and a comprehensive report of the findings. The report not only confirms the presence of any mutations in the ALX4 gene but also provides valuable information for the management of the condition. Families can use this information for planning future pregnancies and understanding the risk of frontonasal dysplasia type 2 in future generations.

For more information about the ALX4 gene frontonasal dysplasia type 2 genetic test and to schedule a test, please visit DNA Labs UAE. Their team of genetic experts is committed to providing accurate, confidential, and comprehensive genetic testing services to help individuals and families understand their genetic health.

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