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PKD1L1 Gene Heterotaxy Visceral Type 8 Autosomal Genetic Test Cost

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

-21%

The PKD1L1 Gene Heterotaxy Visceral Type 8 Autosomal Genetic Test is a specialized diagnostic tool available at DNA Labs UAE. Priced at 4400 AED, this test focuses on identifying mutations in the PKD1L1 gene, which are linked to Heterotaxy Visceral Type 8, a rare genetic disorder. Heterotaxy syndrome is characterized by the abnormal arrangement of internal organs across the left-right axis of the body, which can affect the heart, liver, spleen, and intestines, leading to various health complications.

The test is designed to be comprehensive, utilizing advanced genetic sequencing technologies to detect the presence of autosomal mutations in the PKD1L1 gene. It is primarily recommended for individuals with a clinical diagnosis of heterotaxy or those with a family history of the disorder, aiming to provide a definitive genetic diagnosis. This information is crucial for understanding the condition’s implications, enabling personalized treatment plans, and assessing the risk of passing the genetic mutation to future generations.

DNA Labs UAE, where this test is conducted, is known for its state-of-the-art facilities and expertise in genetic diagnostics, ensuring high accuracy and reliability of test results. The test is a significant step forward in the management and understanding of Heterotaxy Visceral Type 8, offering hope and guidance to affected individuals and their families.

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PKD1L1 Gene Heterotaxy Visceral Type 8 Autosomal Genetic Test

At DNA Labs UAE, we offer the PKD1L1 Gene Heterotaxy Visceral Type 8 Autosomal Genetic Test at a cost of AED 4400.0. This test is used to diagnose the condition and identify any genetic variations or mutations that may be responsible for it.

Test Components

Price: AED 4400.0

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 PKD1L1 Gene Heterotaxy Visceral Type 8 Autosomal Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the condition. This will help in understanding the inheritance pattern and the potential genetic cause.

Test Details

The PKD1L1 gene is associated with a condition called heterotaxy, visceral type 8. Heterotaxy refers to the abnormal arrangement or positioning of internal organs in the body. In this specific type, the condition is inherited in an autosomal recessive manner, meaning that both copies of the gene must be mutated to develop the condition.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous sequencing of multiple genes or even the entire genome. It is used to identify genetic variations or mutations that may be responsible for a particular condition or disease. Therefore, an NGS genetic test for the PKD1L1 gene would involve sequencing the gene to identify any variations or mutations that may be present.

This test can help in the diagnosis of heterotaxy, visceral type 8 and provide information about the genetic cause of the condition. It can also be used for carrier testing or prenatal testing in families with a history of this condition.

Test Name PKD1L1 Gene Heterotaxy visceral type 8 autosomal 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 PKD1L1 Gene Heterotaxy, visceral type 8, autosomal NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PKD1L1 Gene Heterotaxy, visceral type 8, autosomal NGS Genetic DNA Test gene PKD1L1
Test Details

The PKD1L1 gene is associated with a condition called heterotaxy, visceral type 8. Heterotaxy refers to the abnormal arrangement or positioning of internal organs in the body. In this specific type, the condition is inherited in an autosomal recessive manner, meaning that both copies of the gene must be mutated to develop the condition.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous sequencing of multiple genes or even the entire genome. It is used to identify genetic variations or mutations that may be responsible for a particular condition or disease.

Therefore, an NGS genetic test for PKD1L1 gene would involve sequencing the gene to identify any variations or mutations that may be present. This test can help in the diagnosis of heterotaxy, visceral type 8 and provide information about the genetic cause of the condition. It can also be used for carrier testing or prenatal testing in families with a history of this condition.

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