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ANOS1 Gene Kallmann Syndrome Type 1 Genetic Test Cost

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

-21%

The ANOS1 gene Kallmann Syndrome Type 1 genetic test is a specialized diagnostic tool used to identify mutations in the ANOS1 gene, which are responsible for Kallmann Syndrome Type 1. This condition is characterized by a combination of delayed or absent puberty and an impaired sense of smell (anosmia). The test is crucial for confirming the diagnosis, allowing for appropriate management and treatment of the condition. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test provides accurate and reliable results. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to perform this genetic analysis. By identifying the specific genetic mutation, this test plays a vital role in understanding the condition better and tailoring personalized treatment plans for affected individuals.

Description

ANOS1 Gene Kallmann Syndrome Type 1 Genetic Test

Test Name: ANOS1 Gene Kallmann Syndrome Type 1 Genetic Test

Components: ANOS1 Gene Kallmann Syndrome 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: Hepatology, Nephrology, Endocrinology Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for ANOS1 Gene Kallmann Syndrome Type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ANOS1 Gene Kallmann Syndrome Type 1 NGS Genetic DNA Test gene ANOS1

Test Details: The ANOS1 gene, also known as the KAL1 gene, is associated with Kallmann syndrome type 1. Kallmann syndrome is a rare genetic disorder characterized by the combination of delayed or absent puberty and an impaired sense of smell (anosmia or hyposmia). NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the context of Kallmann syndrome type 1, NGS genetic testing involves sequencing the ANOS1 gene to identify any mutations or variations that may be causing the disorder.

The NGS test for ANOS1 gene mutations can be helpful in diagnosing Kallmann syndrome type 1 and determining the underlying genetic cause. It can also be used for carrier testing and genetic counseling for individuals with a family history of the disorder. The test involves obtaining a DNA sample, typically through a blood or saliva sample, and analyzing the sequence of the ANOS1 gene using advanced sequencing technologies. The results are then interpreted by genetic specialists to identify any mutations or variations that may be contributing to the development of Kallmann syndrome type 1.

NGS genetic testing for ANOS1 gene mutations can provide important information for diagnosis, treatment, and genetic counseling for individuals with Kallmann syndrome type 1. It can help guide personalized treatment plans and provide information about the risk of passing the condition on to future generations.

Test Name	ANOS1 Gene Kallmann syndrome 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	Hepatology Nephrology Endocrinology Disorders
Doctor	General Physician
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for ANOS1 Gene Kallmann syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ANOS1 Gene Kallmann syndrome type 1 NGS Genetic DNA Test gene ANOS1
Test Details	ANOS1 gene, also known as KAL1 gene, is associated with Kallmann syndrome type 1. Kallmann syndrome is a rare genetic disorder characterized by the combination of delayed or absent puberty and an impaired sense of smell (anosmia or hyposmia). NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the context of Kallmann syndrome type 1, NGS genetic testing involves sequencing the ANOS1 gene to identify any mutations or variations that may be causing the disorder. The NGS test for ANOS1 gene mutations can be helpful in diagnosing Kallmann syndrome type 1 and determining the underlying genetic cause. It can also be used for carrier testing and genetic counseling for individuals with a family history of the disorder. The test involves obtaining a DNA sample, typically through a blood or saliva sample, and analyzing the sequence of the ANOS1 gene using advanced sequencing technologies. The results are then interpreted by genetic specialists to identify any mutations or variations that may be contributing to the development of Kallmann syndrome type 1. NGS genetic testing for ANOS1 gene mutations can provide important information for diagnosis, treatment, and genetic counseling for individuals with Kallmann syndrome type 1. It can help guide personalized treatment plans and provide information about the risk of passing the condition on to future generations.