Symptoms and Testing information for MIR17HG Gene Feingold syndrome type 2 Genetic Test

Symptoms and Testing information for MIR17HG Gene Feingold syndrome type 2 Genetic Test

Symptoms of MIR17HG Gene Feingold Syndrome Type 2 Genetic Test

Feingold syndrome type 2, a rare genetic disorder, is caused by mutations in the MIR17HG gene. This condition is characterized by a spectrum of physical and developmental anomalies. Understanding the symptoms is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for Feingold syndrome type 2, aimed at detecting mutations in the MIR17HG gene. The cost of this genetic test is 4400 AED.

Key Symptoms of Feingold Syndrome Type 2

The symptoms of Feingold syndrome type 2 can vary widely among affected individuals, but there are several key features that are commonly observed. These include:

  • Microcephaly: A condition where the head and brain are significantly smaller than expected for an individual’s age and sex, potentially leading to developmental delays.
  • Digital Anomalies: These may include short fingers and toes (brachydactyly), missing digits (oligodactyly), or webbed fingers or toes (syndactyly).
  • Gastrointestinal Atresias: This refers to the development of a blockage in the intestines, which can lead to severe digestive problems.
  • Learning Disabilities and Developmental Delays: Individuals with Feingold syndrome type 2 may experience a range of cognitive, speech, and motor delays.
  • Hearing Loss: Some individuals may experience varying degrees of hearing impairment.
  • Growth Retardation: Affected individuals may have reduced growth rates, leading to short stature.

It is important to note that not all individuals with Feingold syndrome type 2 will exhibit all of these symptoms, and the severity can vary significantly.

Importance of Genetic Testing for Feingold Syndrome Type 2

Genetic testing for Feingold syndrome type 2 is critical for several reasons. Firstly, it can provide a definitive diagnosis, distinguishing Feingold syndrome from other syndromes with similar features. Secondly, it enables early intervention and management of symptoms, improving the quality of life for affected individuals. Finally, genetic testing can inform family planning decisions for affected families.

The genetic test offered by DNA Labs UAE for Feingold syndrome type 2 involves analyzing the MIR17HG gene for mutations known to cause the condition. This test is priced at 4400 AED and is a valuable tool for families seeking answers about this rare genetic disorder.

Conclusion

Feingold syndrome type 2 is a complex condition with a wide range of symptoms. Early diagnosis through genetic testing is crucial for managing the condition effectively. DNA Labs UAE is committed to providing accurate and comprehensive genetic testing services, including the MIR17HG gene Feingold syndrome type 2 genetic test. For more information on this test, please visit our website.

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