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AMH Gene Persistent Mullerian duct syndrome type 1 Genetic Test

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

-21%

The “AMH Gene Persistent Mullerian Duct Syndrome Type 1 Genetic Test” is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the Anti-Müllerian Hormone (AMH) gene. This condition, known as Persistent Müllerian Duct Syndrome (PMDS) type 1, is a rare form of intersex disorder where individuals with a typically male XY chromosome pattern exhibit both male and female internal reproductive organs due to the failure of the Müllerian ducts to regress during fetal development. The AMH gene plays a crucial role in this process, and mutations can lead to the syndrome.

The test is priced at 4400 AED and is conducted in the state-of-the-art facilities of DNA Labs UAE, which is equipped with advanced genetic testing technologies. By analyzing the patient’s DNA, the test can identify specific mutations in the AMH gene, providing essential information for diagnosis, management, and counseling of affected individuals and their families. This genetic test is vital for understanding the underlying genetic cause of PMDS type 1 and can aid in the appropriate clinical management of the condition.

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AMH Gene Persistent Mullerian Duct Syndrome Type 1 Genetic Test

Test Name: AMH Gene Persistent Mullerian duct syndrome type 1 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Reproductive Disorders

Doctor: Gynecology

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for AMH Gene Persistent Mullerian duct syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with AMH Gene Persistent Mullerian duct syndrome type 1 NGS Genetic DNA Test gene AMH

Test Details

AMH Gene Persistent Mullerian Duct Syndrome Type 1 NGS Genetic Test is a genetic test that analyzes the AMH gene for mutations or variations associated with Persistent Mullerian Duct Syndrome Type 1 (PMDS1). PMDS1 is a rare genetic disorder that affects sexual development in individuals with XY chromosomes.

The anti-Mullerian hormone (AMH) gene is responsible for producing a protein called anti-Mullerian hormone, which plays a crucial role in the development of male reproductive organs and the regression of female reproductive organs during embryonic development.

This genetic test uses Next-Generation Sequencing (NGS) technology to analyze the AMH gene and identify any mutations or variations that may be present. NGS allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variations associated with PMDS1.

By identifying mutations or variations in the AMH gene, this test can help in the diagnosis of PMDS1 and provide valuable information for genetic counseling and family planning. It can also aid in understanding the underlying genetic mechanisms of PMDS1 and potentially guide treatment decisions.

It is important to note that this test is typically performed in specialized genetic testing laboratories and requires a healthcare provider’s order. Genetic counseling is often recommended before and after the test to discuss the implications of the results and provide support to individuals and families undergoing testing.

Test Name AMH Gene Persistent Mullerian duct 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 Reproductive Disorders
Doctor Gynecology
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for AMH Gene Persistent Mullerian duct syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with AMH Gene Persistent Mullerian duct syndrome type 1 NGS Genetic DNA Test gene AMH
Test Details

AMH Gene Persistent Mllerian Duct Syndrome Type 1 NGS Genetic Test is a genetic test that analyzes the AMH gene for mutations or variations associated with Persistent Mllerian Duct Syndrome Type 1 (PMDS1). PMDS1 is a rare genetic disorder that affects sexual development in individuals with XY chromosomes.

The anti-Mllerian hormone (AMH) gene is responsible for producing a protein called anti-Mllerian hormone, which plays a crucial role in the development of male reproductive organs and the regression of female reproductive organs during embryonic development.

This genetic test uses Next-Generation Sequencing (NGS) technology to analyze the AMH gene and identify any mutations or variations that may be present. NGS allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of genetic variations associated with PMDS1.

By identifying mutations or variations in the AMH gene, this test can help in the diagnosis of PMDS1 and provide valuable information for genetic counseling and family planning. It can also aid in understanding the underlying genetic mechanisms of PMDS1 and potentially guide treatment decisions.

It is important to note that this test is typically performed in specialized genetic testing laboratories and requires a healthcare provider’s order. Genetic counseling is often recommended before and after the test to discuss the implications of the results and provide support to individuals and families undergoing testing.