Adermatoglyphia, often dubbed as the “immigration delay disease,” is a rare genetic disorder characterized by the absence of fingerprints. This condition not only presents unique challenges in personal identification but also raises intriguing questions about genetic inheritance and variability. At DNA Labs UAE, we offer a comprehensive genetic test for the SMARCAD1 gene, which is linked to adermatoglyphia. Understanding the symptoms and implications of this condition is crucial for individuals who might be affected or carry the gene.
Symptoms of Adermatoglyphia
Adermatoglyphia primarily manifests through the absence of fingerprints, a feature that is unique to every individual. However, the condition might also be associated with other less noticeable symptoms. These can include:
- Reduced number of sweat glands on the hands, which can affect the body’s cooling mechanism.
- Slight differences in skin thickness on the fingers, although this can be subtle and not easily noticeable.
- Potential issues with grip due to the lack of ridges on the fingers, although this is not commonly reported.
It is important to note that the absence of fingerprints does not typically lead to any severe health issues. However, it can pose significant challenges in activities and processes that require fingerprint identification.
Understanding the SMARCAD1 Gene
The SMARCAD1 gene plays a pivotal role in the development of fingerprints during fetal development. Mutations in this gene can disrupt the normal pattern formation, leading to adermatoglyphia. The condition is inherited in an autosomal dominant pattern, meaning that only one copy of the altered gene in each cell is sufficient to cause the disorder.
Genetic Testing for Adermatoglyphia
At DNA Labs UAE, we recognize the importance of accurate genetic testing for conditions like adermatoglyphia. Our SMARCAD1 Gene Adermatoglyphia Genetic Test is designed to identify mutations in the SMARCAD1 gene, providing valuable information for affected individuals and their families. The test involves a simple sample collection process, followed by detailed analysis in our state-of-the-art laboratory facilities.
Test Cost
The cost of the SMARCAD1 Gene Adermatoglyphia Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to accurately detect the presence of the SMARCAD1 gene mutation. Given the rarity of the condition and the specialized nature of the test, this cost ensures access to reliable and conclusive results.
Conclusion
Understanding the genetic basis of adermatoglyphia and the symptoms associated with the SMARCAD1 gene mutation is essential for affected individuals. The absence of fingerprints can have practical implications, but with accurate genetic testing, individuals can gain insights into their condition. DNA Labs UAE is committed to providing accessible and precise genetic testing services, including the SMARCAD1 Gene Adermatoglyphia Genetic Test, to help individuals and families navigate the complexities of genetic inheritance.
