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NOTCH2 Gene Alagille Syndrome Type 2 Genetic Test Cost

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

-21%

The NOTCH2 Gene Alagille Syndrome Type 2 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the NOTCH2 gene, which are associated with Alagille Syndrome Type 2. Alagille Syndrome is a genetic disorder that can affect the liver, heart, skeleton, eyes, and kidneys, and its symptoms vary widely among individuals. The NOTCH2 gene plays a crucial role in the development and function of these organs and systems. Identifying mutations in this gene can confirm a diagnosis of Alagille Syndrome Type 2, enabling healthcare providers to tailor medical management and treatment plans more effectively to the needs of the patient.

This test is particularly valuable for individuals showing symptoms of the syndrome or those with a family history of the condition, offering them crucial insights into their genetic health. Conducted at the state-of-the-art facilities of DNA Labs UAE, the test ensures accuracy, confidentiality, and the highest standards of genetic counseling support.

The cost of the NOTCH2 Gene Alagille Syndrome Type 2 Genetic Test is set at 4400 AED. This investment covers the comprehensive process of collecting a DNA sample, usually through a blood draw or cheek swab, and the detailed analysis conducted by experienced geneticists. Patients considering this test are advised to consult with their healthcare providers to understand its implications fully and how its results may influence their medical care and lifestyle choices.

Description

NOTCH2 Gene Alagille Syndrome Type 2 Genetic Test

Components: NOTCH2 Gene Alagille syndrome type 2 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: Clinical History of Patient who is going for NOTCH2 Gene Alagille syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NOTCH2 Gene Alagille syndrome type 2 NGS Genetic DNA Test gene NOTCH2

Test Details: The NOTCH2 gene is associated with Alagille syndrome type 2, a rare genetic disorder characterized by liver, heart, eye, and skeletal abnormalities. Next-generation sequencing (NGS) genetic testing can be used to analyze the NOTCH2 gene and identify any mutations or variations that may be present. NGS genetic testing involves sequencing the DNA of an individual to identify any changes or mutations in specific genes. This can help in the diagnosis of genetic disorders, including Alagille syndrome type 2. By analyzing the NOTCH2 gene, NGS testing can determine if there are any variations or mutations that may be causing the syndrome. Genetic testing for Alagille syndrome type 2 can be done through a blood or saliva sample. The sample is sent to a laboratory where the DNA is extracted and analyzed using NGS technology. The results are then interpreted by geneticists or genetic counselors to determine if there are any pathogenic or disease-causing variants in the NOTCH2 gene. It is important to note that genetic testing for Alagille syndrome type 2 should be performed by a healthcare professional with expertise in genetics. They can provide guidance on the appropriateness of testing, explain the potential benefits and limitations, and help interpret the results in the context of an individual’s specific situation.

Test Name	NOTCH2 Gene Alagille syndrome 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 NOTCH2 Gene Alagille syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NOTCH2 Gene Alagille syndrome type 2 NGS Genetic DNA Test gene NOTCH2
Test Details	The NOTCH2 gene is associated with Alagille syndrome type 2, a rare genetic disorder characterized by liver, heart, eye, and skeletal abnormalities. Next-generation sequencing (NGS) genetic testing can be used to analyze the NOTCH2 gene and identify any mutations or variations that may be present. NGS genetic testing involves sequencing the DNA of an individual to identify any changes or mutations in specific genes. This can help in the diagnosis of genetic disorders, including Alagille syndrome type 2. By analyzing the NOTCH2 gene, NGS testing can determine if there are any variations or mutations that may be causing the syndrome. Genetic testing for Alagille syndrome type 2 can be done through a blood or saliva sample. The sample is sent to a laboratory where the DNA is extracted and analyzed using NGS technology. The results are then interpreted by geneticists or genetic counselors to determine if there are any pathogenic or disease-causing variants in the NOTCH2 gene. It is important to note that genetic testing for Alagille syndrome type 2 should be performed by a healthcare professional with expertise in genetics. They can provide guidance on the appropriateness of testing, explain the potential benefits and limitations, and help interpret the results in the context of an individual’s specific situation.