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MIR17HG Gene Feingold syndrome type 2 Genetic Test Cost

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

-21%

The MIR17HG gene, associated with Feingold syndrome type 2, is a critical focus for genetic testing at DNA Labs UAE. Feingold syndrome type 2 is a rare genetic disorder characterized by various anomalies, including digital and gastrointestinal abnormalities. The condition is inherited in an autosomal dominant manner, meaning a mutation in just one copy of the gene in each cell is sufficient to cause the disorder.

DNA Labs UAE offers a specialized genetic test to identify mutations in the MIR17HG gene, providing essential information for the diagnosis, management, and genetic counseling of affected families. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing the genetic material for specific mutations associated with Feingold syndrome type 2.

The cost of the MIR17HG gene test for Feingold syndrome type 2 at DNA Labs UAE is 4400 AED. This comprehensive test is a valuable tool for families seeking answers about this rare condition, enabling them to make informed decisions about their health and future.

Description

MIR17HG Gene Feingold Syndrome Type 2 Genetic Test

Test Name: MIR17HG Gene Feingold syndrome type 2 Genetic Test

Components: DNA Labs UAE

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: Osteology Dermatology Immunology Disorders

Doctor: Dermatologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for MIR17HG Gene Feingold syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MIR17HG Gene Feingold syndrome type 2 NGS Genetic DNA Test gene MIR17HG

Test Details:

The MIR17HG gene is a gene located on chromosome 13 that encodes for a microRNA. MicroRNAs are small RNA molecules that play a role in regulating gene expression.

Feingold syndrome type 2 is a rare genetic disorder characterized by various physical abnormalities, such as hand and foot abnormalities, microcephaly (small head size), and gastrointestinal and cardiac defects. It is caused by mutations in the MIR17HG gene.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously for mutations or variants. In the case of Feingold syndrome type 2, NGS genetic testing can be used to identify mutations in the MIR17HG gene.

The test involves obtaining a DNA sample, usually through a blood sample, and sequencing the DNA using NGS technology. The sequencing data is then analyzed to identify any mutations or variants in the MIR17HG gene that may be causing Feingold syndrome type 2.

NGS genetic testing for Feingold syndrome type 2 can help in confirming a diagnosis, guiding treatment decisions, and providing genetic counseling for affected individuals and their families.

Test Name	MIR17HG Gene Feingold syndrome type 2 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	Osteology Dermatology Immunology Disorders
Doctor	Dermatologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for MIR17HG Gene Feingold syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MIR17HG Gene Feingold syndrome type 2 NGS Genetic DNA Test gene MIR17HG
Test Details	The MIR17HG gene is a gene located on chromosome 13 that encodes for a microRNA. MicroRNAs are small RNA molecules that play a role in regulating gene expression. Feingold syndrome type 2 is a rare genetic disorder characterized by various physical abnormalities, such as hand and foot abnormalities, microcephaly (small head size), and gastrointestinal and cardiac defects. It is caused by mutations in the MIR17HG gene. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously for mutations or variants. In the case of Feingold syndrome type 2, NGS genetic testing can be used to identify mutations in the MIR17HG gene. The test involves obtaining a DNA sample, usually through a blood sample, and sequencing the DNA using NGS technology. The sequencing data is then analyzed to identify any mutations or variants in the MIR17HG gene that may be causing Feingold syndrome type 2. NGS genetic testing for Feingold syndrome type 2 can help in confirming a diagnosis, guiding treatment decisions, and providing genetic counseling for affected individuals and their families.