Symptoms of Maternal UPD Chr. 14 Gene Temple Syndrome Genetic Test
Maternal Uniparental Disomy of Chromosome 14 (matUPD(14)) is a rare genetic condition, often associated with a constellation of physical and developmental symptoms known as Temple Syndrome. This condition arises when a child inherits two copies of chromosome 14 from the mother and none from the father. Recognizing the symptoms early can lead to timely intervention and management, enhancing the quality of life for those affected. DNA Labs UAE offers a comprehensive genetic test for Maternal UPD Chr. 14 Gene Temple Syndrome, priced at 4400 AED, to assist in the diagnosis of this rare condition.
Key Symptoms of Temple Syndrome
Temple Syndrome presents a range of symptoms that can vary significantly from one individual to another. However, some common signs include:
- Growth retardation: Affected individuals may exhibit growth retardation, both prenatally and postnatally, leading to short stature.
- Muscle hypotonia: Low muscle tone or muscle weakness is a common symptom, which may contribute to delayed developmental milestones.
- Early-onset puberty: Children with Temple Syndrome may experience precocious puberty, starting puberty earlier than is typically expected.
- Feeding difficulties: Infants may face challenges with feeding, including poor sucking ability and failure to thrive in the early months of life.
- Distinctive facial features: Some individuals may have facial characteristics that are unique to Temple Syndrome, such as a prominent forehead, a small lower jaw, and a thin upper lip.
- Developmental delays: There can be delays in reaching developmental milestones, including sitting, walking, and talking.
- Behavioral issues: Children may exhibit behavioral problems, including temper tantrums, stubbornness, and obsessive-compulsive behaviors.
It is crucial to note that not all individuals with Temple Syndrome will exhibit all of these symptoms, and the severity can vary widely.
Importance of Genetic Testing for Temple Syndrome
Genetic testing plays a pivotal role in the diagnosis of Temple Syndrome. The Maternal UPD Chr. 14 Gene Temple Syndrome Genetic Test offered by DNA Labs UAE is a vital tool in confirming the diagnosis of this condition. Early diagnosis through genetic testing can facilitate early intervention strategies, tailored therapies, and support to improve developmental outcomes and manage symptoms effectively.
Understanding the Test
The genetic test for Temple Syndrome at DNA Labs UAE involves analyzing the individual’s DNA to look for the specific pattern of inheritance that characterizes maternal UPD(14). This test, priced at 4400 AED, is conducted with a high degree of accuracy and sensitivity, ensuring reliable results. The process is straightforward, requiring only a simple sample collection that can be performed with minimal discomfort.
For more information on the Maternal UPD Chr. 14 Gene Temple Syndrome Genetic Test, including how to book your test, please visit https://dnalabsuae.com/tests/maternal-upd-chr-14-gene-temple-syndrome-genetic-test/.
Conclusion
Temple Syndrome, caused by Maternal Uniparental Disomy of Chromosome 14, is a rare genetic condition that can significantly impact an individual’s growth, development, and overall quality of life. Recognizing the symptoms early and undergoing genetic testing, such as the Maternal UPD Chr. 14 Gene Temple Syndrome Genetic Test offered by DNA Labs UAE, is crucial for accurate diagnosis and management. With a comprehensive understanding of the condition and access to specialized care, individuals with Temple Syndrome can lead fulfilling lives.
