Craniosynostosis Type 3, also known as Saethre-Chotzen syndrome, is a genetic condition characterized by the premature fusion of certain skull bones. This early fusion prevents the skull from growing normally and affects the shape of the head and face. It is caused by mutations in the TCF12 gene. Understanding the symptoms of this condition is crucial for early diagnosis and treatment. DNA Labs UAE offers a comprehensive genetic test for TCF12 Gene Craniosynostosis Type 3, aimed at providing accurate diagnosis for affected individuals and their families.
Symptoms of TCF12 Gene Craniosynostosis Type 3
Recognizing the symptoms of TCF12 Gene Craniosynostosis Type 3 is essential for early intervention. The symptoms can vary from one individual to another but generally include:
- Abnormal Head Shape: One of the most noticeable signs is an unusual head shape, which may be elongated, flattened at the back, or have a raised ridge along the affected sutures.
- Facial Asymmetry: Due to the premature fusion of skull bones, individuals may experience asymmetry in facial features.
- Wide-Set, Bulging Eyes: The condition can cause the eye sockets to be shallow, making the eyes appear more prominent and possibly wider set than usual.
- Beaked Nose: A beaked nose is another characteristic feature of this condition.
- Low Hairline: Individuals may have a hairline that is lower than usual.
- Short Fingers and Toes: This symptom is not related to the skull but is another sign of TCF12 Gene Craniosynostosis Type 3.
- Developmental Delays: In some cases, affected individuals may experience delays in development or mild to moderate intellectual disability.
It’s important to note that not all individuals with TCF12 Gene Craniosynostosis Type 3 will experience all of these symptoms, and the severity can vary widely.
TCF12 Gene Craniosynostosis Type 3 Genetic Test at DNA Labs UAE
DNA Labs UAE is at the forefront of genetic testing, offering a specialized test for TCF12 Gene Craniosynostosis Type 3. This test is designed to identify mutations in the TCF12 gene that are responsible for the condition. Early diagnosis through genetic testing can provide valuable information for managing the condition, including surgical options to correct the skull shape and prevent complications.
The cost of the TCF12 Gene Craniosynostosis Type 3 Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test is a crucial step towards understanding the genetic basis of the condition and planning the appropriate course of treatment and management.
For more information on the TCF12 Gene Craniosynostosis Type 3 Genetic Test and to schedule your test, please visit DNA Labs UAE.
Early diagnosis and intervention are key to managing TCF12 Gene Craniosynostosis Type 3 effectively. With the support of DNA Labs UAE, individuals and families affected by this condition can gain access to crucial genetic information that will aid in making informed decisions about their health and treatment options.
