Symptoms and Testing information for ZSWIM6 Gene Acromelic Frontonasal Dysostosis Genetic Test

Symptoms and Testing information for ZSWIM6 Gene Acromelic Frontonasal Dysostosis Genetic Test

Acromelic Frontonasal Dysostosis (AFND) is a rare genetic disorder that affects the development of the head, face, and limbs. This condition is characterized by a range of physical anomalies, including craniofacial, limb, and brain abnormalities. Recent studies have identified mutations in the ZSWIM6 gene as a significant cause of AFND. DNA Labs UAE offers a comprehensive genetic test for the ZSWIM6 gene to help diagnose this condition. The cost of the test is 4400 AED.

Understanding Acromelic Frontonasal Dysostosis

Acromelic Frontonasal Dysostosis is a condition that presents with distinct facial and limb features. Individuals with AFND may have a broadened nasal tip, widely spaced eyes (hypertelorism), a large forehead, and abnormalities in the development of the arms and legs. In addition to physical symptoms, some affected individuals may experience cognitive delays or neurological issues.

Significance of the ZSWIM6 Gene

The ZSWIM6 gene plays a crucial role in the early development of the craniofacial region and limb formation. Mutations in this gene disrupt normal development, leading to the characteristics observed in AFND. Genetic testing for mutations in the ZSWIM6 gene can provide definitive diagnosis and help in the management of the condition.

Symptoms of Acromelic Frontonasal Dysostosis

  • Wide spacing between the eyes (hypertelorism)

  • Median cleft lip and palate

  • Broad nasal tip

  • Brachycephaly (short and broad head)

  • Abnormalities in limb development, such as syndactyly (fusion of digits)

  • Neurodevelopmental delays and intellectual disability

ZSWIM6 Gene Acromelic Frontonasal Dysostosis Genetic Test

DNA Labs UAE offers a genetic test specifically designed to detect mutations in the ZSWIM6 gene associated with AFND. The test involves a simple blood sample from the patient and utilizes advanced genomic sequencing techniques to identify mutations. The cost of the test is 4400 AED. Early diagnosis through genetic testing can significantly impact the management and treatment of AFND, offering families better understanding and preparation for the challenges associated with the condition.

Why Choose DNA Labs UAE?

DNA Labs UAE is a leading provider of genetic testing services in the United Arab Emirates. Our state-of-the-art laboratory is equipped with the latest technology for accurate and reliable genetic testing. Our team of expert geneticists and counselors are committed to providing the highest standard of care, from the initial consultation to the delivery of test results.

Conclusion

Acromelic Frontonasal Dysostosis is a complex condition that requires a comprehensive approach for diagnosis and management. The ZSWIM6 gene test offered by DNA Labs UAE represents a crucial step in understanding and addressing this rare disorder. For more information or to schedule a test, please visit our website at DNA Labs UAE.

Understanding Acromelic Frontonasal Dysostosis

Acromelic Frontonasal Dysostosis is a condition that presents with distinct facial and limb features. Individuals with AFND may have a broadened nasal tip, widely spaced eyes (hypertelorism), a large forehead, and abnormalities in the development of the arms and legs. In addition to physical symptoms, some affected individuals may experience cognitive delays or neurological issues.

Significance of the ZSWIM6 Gene

The ZSWIM6 gene plays a crucial role in the early development of the craniofacial region and limb formation. Mutations in this gene disrupt normal development, leading to the characteristics observed in AFND. Genetic testing for mutations in the ZSWIM6 gene can provide definitive diagnosis and help in the management of the condition.

Symptoms of Acromelic Frontonasal Dysostosis

  • Wide spacing between the eyes (hypertelorism)

  • Median cleft lip and palate

  • Broad nasal tip

  • Brachycephaly (short and broad head)

  • Abnormalities in limb development, such as syndactyly (fusion of digits)

  • Neurodevelopmental delays and intellectual disability

ZSWIM6 Gene Acromelic Frontonasal Dysostosis Genetic Test

DNA Labs UAE offers a genetic test specifically designed to detect mutations in the ZSWIM6 gene associated with AFND. The test involves a simple blood sample from the patient and utilizes advanced genomic sequencing techniques to identify mutations. The cost of the test is 4400 AED. Early diagnosis through genetic testing can significantly impact the management and treatment of AFND, offering families better understanding and preparation for the challenges associated with the condition.

Why Choose DNA Labs UAE?

DNA Labs UAE is a leading provider of genetic testing services in the United Arab Emirates. Our state-of-the-art laboratory is equipped with the latest technology for accurate and reliable genetic testing. Our team of expert geneticists and counselors are committed to providing the highest standard of care, from the initial consultation to the delivery of test results.

Conclusion

Acromelic Frontonasal Dysostosis is a complex condition that requires a comprehensive approach for diagnosis and management. The ZSWIM6 gene test offered by DNA Labs UAE represents a crucial step in understanding and addressing this rare disorder. For more information or to schedule a test, please visit our website at DNA Labs UAE.

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