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MYCN Gene Feingold Syndrome Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The MYCN Gene Feingold Syndrome Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the MYCN gene, which are associated with Feingold syndrome. Feingold syndrome is a rare genetic disorder characterized by microcephaly (small head size), short stature, digital anomalies (such as missing or underdeveloped fingers or toes), and gastrointestinal atresia, among other symptoms. The test plays a crucial role in the early detection and management of the syndrome, enabling healthcare providers to offer targeted interventions and support to affected individuals and their families.

Performed at the state-of-the-art facilities of DNA Labs UAE, this genetic test involves analyzing the patient’s DNA to look for specific mutations in the MYCN gene that are known to cause Feingold syndrome. The process is highly accurate and provides vital information for the diagnosis and understanding of the condition. The test is priced at 4400 AED, reflecting the advanced technology and expertise required to accurately identify the presence of the MYCN gene mutations.

By opting for the MYCN Gene Feingold Syndrome Genetic Test, patients and their families can gain valuable insights into the genetic basis of the condition, paving the way for personalized care plans and interventions. DNA Labs UAE ensures confidentiality, precision, and comprehensive support throughout the testing process, making it a trusted choice for genetic diagnostics in the region.

Description

MYCN Gene Feingold syndrome Genetic Test

Test Name: MYCN Gene Feingold syndrome Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for MYCN Gene Feingold syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYCN Gene Feingold syndrome NGS Genetic DNA Test gene MYCN

Test Details:

The MYCN gene is a gene that encodes a protein called N-myc, which plays a role in cell growth and development. Mutations or alterations in the MYCN gene can lead to various genetic disorders or syndromes.

Feingold syndrome is a rare genetic disorder characterized by a combination of physical abnormalities and intellectual disability. It is caused by mutations in several genes, including the MYCN gene.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the rapid and efficient detection of genetic variants, including mutations in the MYCN gene, associated with Feingold syndrome.

NGS genetic testing can help in the diagnosis of Feingold syndrome by identifying mutations or alterations in the MYCN gene and other relevant genes. It can also provide information about the specific genetic variant present, which can be helpful for understanding the underlying cause of the syndrome and for genetic counseling purposes.

Overall, NGS genetic testing for the MYCN gene and Feingold syndrome can aid in the accurate diagnosis, management, and counseling of individuals and families affected by this rare genetic disorder.

Test Name	MYCN Gene Feingold syndrome Genetic Test
Components
Price	4400.0 AED
Sample Condition	Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery	3 to 4 Weeks
Method	NGS Technology
Test type	Dysmorphology
Doctor	Pediatrics
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for MYCN Gene Feingold syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYCN Gene Feingold syndrome NGS Genetic DNA Test gene MYCN
Test Details	The MYCN gene is a gene that encodes a protein called N-myc, which plays a role in cell growth and development. Mutations or alterations in the MYCN gene can lead to various genetic disorders or syndromes. Feingold syndrome is a rare genetic disorder characterized by a combination of physical abnormalities and intellectual disability. It is caused by mutations in several genes, including the MYCN gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the rapid and efficient detection of genetic variants, including mutations in the MYCN gene, associated with Feingold syndrome. NGS genetic testing can help in the diagnosis of Feingold syndrome by identifying mutations or alterations in the MYCN gene and other relevant genes. It can also provide information about the specific genetic variant present, which can be helpful for understanding the underlying cause of the syndrome and for genetic counseling purposes. Overall, NGS genetic testing for the MYCN gene and Feingold syndrome can aid in the accurate diagnosis, management, and counseling of individuals and families affected by this rare genetic disorder.