Deafness congenital with inner ear agenesis, microtia, and microdontia, often abbreviated as DCIA, is a rare genetic disorder. This condition is characterized by a range of symptoms, primarily affecting the ears and teeth, and is caused by mutations in the FGF3 gene. Understanding the symptoms and the availability of genetic testing is crucial for early diagnosis and management of the condition. DNA Labs UAE offers a comprehensive genetic test for this disorder, providing essential information for affected individuals and their families.
Symptoms of FGF3 Gene Deafness Congenital with Inner Ear Agenesis, Microtia, and Microdontia
The symptoms of this genetic disorder are diverse, affecting several parts of the body, but most notably the ears and teeth. The most common symptoms include:
- Inner Ear Agenesis: This is the absence or underdevelopment of the inner ear, leading to hearing loss or deafness from birth. It is one of the primary indicators of the condition.
- Microtia: This refers to the underdevelopment of the external ear, ranging from slight structural abnormalities to complete absence of the ear.
- Microdontia: Affected individuals may have smaller than average teeth, which may also be fewer in number. This can affect both primary (baby) and permanent teeth.
Other symptoms may include difficulties in speech and language development due to hearing impairment, challenges with balance, and potential facial asymmetry due to ear abnormalities. It is important to note that the severity and combination of symptoms can vary significantly among individuals.
Genetic Test for FGF3 Gene Deafness Congenital with Inner Ear Agenesis, Microtia, and Microdontia
DNA Labs UAE offers a specialized genetic test designed to identify mutations in the FGF3 gene, which are responsible for this condition. The test involves a simple sample collection process, after which the sample is analyzed to detect any genetic abnormalities that may indicate the disorder.
The cost of the genetic test is 4400 AED. This comprehensive test not only helps in confirming the diagnosis but also assists in understanding the risk of passing the condition to future generations. Early diagnosis through genetic testing is crucial as it enables timely intervention and management strategies to address the symptoms and improve the quality of life for those affected.
For more information about the genetic test and to schedule a testing appointment, please visit DNA Labs UAE.
Early identification and intervention are key in managing the symptoms associated with FGF3 gene deafness congenital with inner ear agenesis, microtia, and microdontia. With the availability of genetic testing, individuals and families can gain valuable insights into their condition, leading to better-informed decisions about their health and care.
