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BCL9L Gene Heterotaxy Visceral BCL9L Related Genetic Test

Name: BCL9L Gene Heterotaxy Visceral BCL9L Related Genetic Test
SKU: TEST-4144
Price: 4400 AED
Availability: InStock

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

-21%

The BCL9L gene is crucial in the development and arrangement of the body’s organs, particularly in determining their left-right placement, a process known as lateralization. Mutations in the BCL9L gene can lead to heterotaxy, a condition where organs are abnormally arranged across the left-right axis of the body. This can affect various organs, including the heart, liver, and spleen, leading to complex congenital conditions that require careful medical management.

The BCL9L-related genetic test is a specific diagnostic tool used to detect mutations in the BCL9L gene that are associated with heterotaxy and related visceral malformations. This test is essential for early diagnosis, which can significantly impact the management, treatment, and prognosis of affected individuals. By understanding the genetic basis of the condition, healthcare providers can tailor interventions more effectively and provide families with crucial information regarding the condition’s inheritance patterns and potential implications for future pregnancies.

Conducted at DNA Labs UAE, the test is priced at 4400 AED. DNA Labs UAE is a reputable facility known for its comprehensive genetic testing services, employing state-of-the-art technology to ensure accurate and reliable results. The cost of the test reflects the complex nature of genetic analysis and the specialized expertise required to interpret the results. For families facing the possibility of heterotaxy or related conditions, this test represents a critical step in accessing appropriate care and support for their loved ones.

Description

BCL9L Gene Heterotaxy Visceral BCL9L Related Genetic Test

Test Name: BCL9L Gene Heterotaxy Visceral BCL9L Related 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: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for BCL9L Gene Heterotaxy, visceral, BCL9L related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BCL9L Gene Heterotaxy, visceral, BCL9L related NGS Genetic DNA Test gene BCL9L

Test Details: The BCL9L gene is associated with the development of heterotaxy, a condition characterized by abnormal positioning or arrangement of internal organs. Heterotaxy can affect various organs, including the heart, lungs, liver, and intestines. A genetic test focusing on the BCL9L gene can identify mutations or variations in this gene that may be responsible for the development of heterotaxy. This test uses next-generation sequencing (NGS) technology for rapid and accurate analysis of a large number of genes simultaneously. NGS genetic testing for BCL9L-related heterotaxy involves obtaining a DNA sample, typically through a blood sample, and sequencing the DNA to identify variations or mutations in the BCL9L gene. These variations help determine the underlying genetic cause of heterotaxy. The test results provide valuable information for diagnosing and managing heterotaxy, understanding the genetic basis of the condition, assessing the risk of recurrence in family members, and guiding appropriate treatment and management strategies. Genetic testing for BCL9L-related heterotaxy is performed in specialized genetic testing laboratories and requires the guidance and interpretation of a healthcare professional. Genetic counseling is recommended before and after the test to discuss the implications of the results and provide support to individuals and families.

Test Name	BCL9L Gene Heterotaxy visceral BCL9L related 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 BCL9L Gene Heterotaxy, visceral, BCL9L related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BCL9L Gene Heterotaxy, visceral, BCL9L related NGS Genetic DNA Test gene BCL9L
Test Details	The BCL9L gene is a gene that is associated with the development of heterotaxy, a condition characterized by abnormal positioning or arrangement of internal organs. Heterotaxy can affect various organs, including the heart, lungs, liver, and intestines. A genetic test that focuses on the BCL9L gene can be used to identify mutations or variations in this gene that may be responsible for the development of heterotaxy. This test is typically performed using next-generation sequencing (NGS) technology, which allows for the rapid and accurate analysis of a large number of genes simultaneously. NGS genetic testing for BCL9L-related heterotaxy involves obtaining a DNA sample, typically through a blood sample, from the individual being tested. The DNA is then sequenced to identify any variations or mutations in the BCL9L gene. These variations can help in determining the underlying genetic cause of heterotaxy in the individual. The results of the genetic test can provide valuable information for diagnosing and managing heterotaxy. It can help in understanding the genetic basis of the condition, assessing the risk of recurrence in family members, and guiding appropriate treatment and management strategies. It is important to note that genetic testing for BCL9L-related heterotaxy is typically performed in specialized genetic testing laboratories and requires a healthcare professional’s guidance and interpretation of the results. Genetic counseling is often recommended before and after the test to discuss the implications of the results and provide support to individuals and families.