Sale!

ZIC3 Gene Heterotaxy Visceral Type 1 Genetic Test

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

-21%

The ZIC3 Gene Heterotaxy Visceral Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the ZIC3 gene, which are associated with Heterotaxy Visceral Type 1. Heterotaxy syndrome is a rare congenital condition characterized by the abnormal arrangement of internal organs across the left-right axis of the body, which can affect the heart, liver, lungs, and spleen. The condition can lead to significant health issues, including complex congenital heart disease and functional abnormalities of the affected organs.

The test targets individuals who exhibit symptoms of heterotaxy syndrome or have a family history of the condition, providing crucial information for diagnosis, treatment planning, and genetic counseling. By analyzing the ZIC3 gene specifically, the test can pinpoint mutations responsible for the disorder, offering insights into the genetic basis of the patient’s condition.

Priced at 4400 AED, the test is conducted at the state-of-the-art facilities of DNA Labs UAE, which is known for its cutting-edge genetic testing services. The cost reflects the comprehensive nature of the test, including the sophisticated techniques used for genetic analysis, the expertise required to interpret the results accurately, and the personalized care provided to each patient.

Overall, the ZIC3 Gene Heterotaxy Visceral Type 1 Genetic Test represents a critical tool in the diagnosis and management of heterotaxy syndrome, facilitating targeted interventions and supporting affected families in understanding their genetic health landscape.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

ZIC3 Gene Heterotaxy visceral type 1 Genetic Test

At DNA Labs UAE, we offer the ZIC3 Gene Heterotaxy visceral type 1 Genetic Test. This test helps in diagnosing the condition and provides valuable information for medical management and genetic counseling.

Test Components

  • Test Name: ZIC3 Gene Heterotaxy visceral type 1 Genetic Test
  • 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

Before undergoing the ZIC3 Gene Heterotaxy visceral type 1 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected with the ZIC3 Gene Heterotaxy visceral type 1 NGS Genetic DNA Test gene ZIC3.

Test Details

The ZIC3 gene plays a crucial role in the development of the body’s organs, particularly during early embryonic development. Mutations in this gene can result in a rare condition called heterotaxy, visceral type 1. This condition is characterized by abnormalities in the arrangement of internal organs, with organs often being mirror images of each other or misplaced on the opposite side of the body.

Heterotaxy, visceral type 1 can lead to various health problems, including heart defects, liver abnormalities, and digestive system issues. To diagnose this condition, our lab utilizes NGS (Next-Generation Sequencing) technology. NGS genetic testing allows for the rapid analysis of multiple genes simultaneously. It can detect mutations or variations in the ZIC3 gene associated with heterotaxy, visceral type 1.

If a healthcare provider suspects heterotaxy, visceral type 1 in a patient, they may recommend NGS genetic testing. The test involves obtaining a sample of the patient’s DNA, typically through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variations in the ZIC3 gene.

It is important to note that genetic testing for heterotaxy, visceral type 1 is typically performed in specialized laboratories and requires a healthcare provider’s order. Genetic counseling is also recommended before and after testing to help individuals and families understand the implications of the test results and make informed decisions about their healthcare.

Test Name ZIC3 Gene Heterotaxy visceral type 1 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 ZIC3 Gene Heterotaxy, visceral type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ZIC3 Gene Heterotaxy, visceral type 1 NGS Genetic DNA Test gene ZIC3
Test Details

The ZIC3 gene is a gene that provides instructions for making a protein called Zic3. This protein is involved in the development of the body’s organs, particularly during early embryonic development. Mutations in the ZIC3 gene can lead to a condition called heterotaxy, visceral type 1.

Heterotaxy is a rare condition characterized by abnormalities in the arrangement of internal organs. In visceral type 1 heterotaxy, the organs are usually mirror images of each other or are misplaced on the opposite side of the body. This can result in various health problems, including heart defects, liver abnormalities, and problems with the digestive system.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to rapidly analyze multiple genes simultaneously. It can detect mutations or variations in the ZIC3 gene that may be associated with heterotaxy, visceral type 1. NGS testing can help diagnose the condition and provide valuable information for medical management and genetic counseling.

If a healthcare provider suspects heterotaxy, visceral type 1 in a patient, they may recommend NGS genetic testing to confirm the diagnosis. The test involves obtaining a sample of the patient’s DNA, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variations in the ZIC3 gene.

It’s important to note that genetic testing for heterotaxy, visceral type 1 is typically performed in specialized laboratories and requires a healthcare provider’s order. Genetic counseling is also recommended before and after testing to help individuals and families understand the implications of the test results and make informed decisions about their healthcare.