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CFC1 Gene Heterotaxy Visceral Type 2 Genetic Test Cost

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

-21%

The “CFC1 Gene Heterotaxy Visceral Type 2 Genetic Test” is a specialized diagnostic procedure designed to identify mutations in the CFC1 gene, which are associated with Heterotaxy Visceral Type 2, a rare genetic disorder. This condition is characterized by the abnormal arrangement of internal organs across the left-right axis of the body, potentially affecting the heart, liver, spleen, and other organs. The test is crucial for early diagnosis and management of the disorder, offering insights into treatment options and genetic counseling for affected families.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test employs advanced genetic sequencing technologies to accurately detect mutations in the CFC1 gene. The process involves collecting a DNA sample, typically through a blood draw, which is then analyzed in the laboratory for the presence of genetic abnormalities linked to the condition.

The cost of the “CFC1 Gene Heterotaxy Visceral Type 2 Genetic Test” at DNA Labs UAE is set at 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to perform it. For families and individuals facing the possibility of Heterotaxy Visceral Type 2, this test represents a critical step towards understanding their genetic health and making informed decisions about their care.

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CFC1 Gene Heterotaxy Visceral Type 2 Genetic Test

At DNA Labs UAE, we offer the CFC1 Gene Heterotaxy Visceral Type 2 Genetic Test to diagnose and understand the genetic basis of this rare condition. This test is designed to analyze the CFC1 gene and identify any variations or mutations that may be present.

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

Prior to undergoing the CFC1 Gene Heterotaxy Visceral Type 2 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by CFC1 Gene Heterotaxy Visceral Type 2 NGS Genetic DNA Test gene CFC1.

Test Details

The CFC1 gene is associated with a rare genetic disorder called heterotaxy, visceral type 2. This condition affects the formation and arrangement of organs in the body, specifically in the chest and abdomen. The NGS genetic testing method is used to analyze multiple genes simultaneously, allowing for the detection of genetic variations or mutations related to this condition.

Genetic testing can serve various purposes, including confirming a clinical diagnosis, predicting the risk of passing the condition on to future generations, guiding treatment decisions, and providing valuable information for genetic counseling and family planning.

It is crucial to note that genetic testing should always be conducted under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations based on individual circumstances.

Test Name CFC1 Gene Heterotaxy visceral 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for CFC1 Gene Heterotaxy, visceral type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CFC1 Gene Heterotaxy, visceral type 2 NGS Genetic DNA Test gene CFC1
Test Details

The CFC1 gene is associated with a condition called heterotaxy, visceral type 2. Heterotaxy is a rare genetic disorder that affects the formation and arrangement of organs in the body. In particular, it affects the positioning of organs in the chest and abdomen.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of genetic variations or mutations that may be responsible for a particular condition or disease.

In the case of CFC1 gene heterotaxy, visceral type 2, an NGS genetic test would involve sequencing the CFC1 gene to identify any variations or mutations that may be present. This can help in diagnosing the condition and understanding its genetic basis.

Genetic testing can be useful in several ways, including confirming a clinical diagnosis, predicting the risk of passing the condition on to future generations, and guiding treatment decisions. It can also provide valuable information for genetic counseling and family planning.

It’s important to note that genetic testing should always be conducted under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate recommendations based on individual circumstances.

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