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FGFR2 Gene Bent Bone Dysplasia Syndrome Genetic Test Cost

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

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The FGFR2 Gene Bent Bone Dysplasia Syndrome Genetic Test is a specialized diagnostic examination offered at DNA Labs UAE, designed to identify mutations in the FGFR2 gene, which are linked to Bent Bone Dysplasia Syndrome. This condition is a rare genetic disorder characterized by skeletal abnormalities, including significantly bent bones, underdeveloped lungs, and other potential complications that can affect a patient’s quality of life from a very early age. The test, priced at 4400 AED, involves analyzing the patient’s DNA to detect specific genetic alterations in the FGFR2 gene, providing crucial information for accurate diagnosis, management, and genetic counseling for affected families. Conducted in the state-of-the-art facilities of DNA Labs UAE, this test is a vital tool for healthcare providers and families seeking to understand the genetic basis of Bent Bone Dysplasia Syndrome and related skeletal disorders.

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FGFR2 Gene Bent bone dysplasia syndrome Genetic Test

Are you concerned about Bent bone dysplasia syndrome (BBDS) and its genetic implications? DNA Labs UAE offers a comprehensive FGFR2 Gene Bent bone dysplasia syndrome Genetic Test to provide you with the answers you need.

Test Details

The FGFR2 gene is associated with a condition called Bent bone dysplasia syndrome (BBDS). BBDS is a rare genetic disorder characterized by skeletal abnormalities, including bent bones, craniofacial anomalies, and short stature.

Our Next-Generation Sequencing (NGS) technology allows us to analyze multiple genes simultaneously, including the FGFR2 gene, to identify mutations or variations that may be associated with BBDS.

Test Components and Price

Our FGFR2 Gene Bent bone dysplasia syndrome Genetic Test is priced at 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 FGFR2 Gene Bent bone dysplasia syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene Bent bone dysplasia syndrome NGS Genetic DNA Test gene FGFR2.

Why Choose NGS Genetic Testing?

NGS testing involves sequencing the DNA of an individual, typically using a blood or saliva sample, to identify any changes or mutations in the FGFR2 gene. This can help in confirming a diagnosis of BBDS and can also provide information about the specific genetic variant causing the condition.

By opting for our FGFR2 Gene Bent bone dysplasia syndrome Genetic Test, you can gain valuable insights for genetic counseling, family planning, and potentially for guiding treatment decisions in the future.

Don’t let the uncertainties surrounding BBDS weigh you down. Take control of your genetic health today with DNA Labs UAE’s FGFR2 Gene Bent bone dysplasia syndrome Genetic Test.

Test Name FGFR2 Gene Bent bone dysplasia 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FGFR2 Gene Bent bone dysplasia syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene Bent bone dysplasia syndrome NGS Genetic DNA Test gene FGFR2
Test Details

The FGFR2 gene is associated with a condition called Bent bone dysplasia syndrome (BBDS). BBDS is a rare genetic disorder characterized by skeletal abnormalities, including bent bones, craniofacial anomalies, and short stature.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously to identify mutations or variations that may be associated with a particular condition. In the case of BBDS, NGS testing can be used to detect mutations or variations in the FGFR2 gene that are responsible for causing the condition.

NGS testing involves sequencing the DNA of an individual, typically using a blood or saliva sample, to identify any changes or mutations in the FGFR2 gene. This can help in confirming a diagnosis of BBDS and can also provide information about the specific genetic variant causing the condition. This information can be useful for genetic counseling, family planning, and potentially for guiding treatment decisions in the future.

SKU: TEST-2874 Category:

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