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WNT4 Gene SERKAL syndrome Genetic Test Cost

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

-21%

The WNT4 Gene SERKAL Syndrome Genetic Test is a specialized diagnostic tool designed to identify mutations in the WNT4 gene, which are associated with SERKAL syndrome. SERKAL syndrome is a rare genetic disorder characterized by a spectrum of abnormalities including renal, skeletal, and genital malformations. This condition is inherited in an autosomal dominant manner, meaning a mutation in just one of the two copies of the gene can cause the disorder.

DNA Labs UAE offers this comprehensive genetic test as part of their advanced diagnostic services to help detect the presence of WNT4 gene mutations. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory using sophisticated genetic sequencing technologies. This allows for the precise identification of mutations in the WNT4 gene that are indicative of SERKAL syndrome.

The cost of the WNT4 Gene SERKAL Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the intricate nature of the genetic analysis and the valuable insights it provides for affected individuals and their families. By confirming a diagnosis, this test can guide clinical management, inform family planning decisions, and enable access to targeted therapies and support services, significantly impacting the quality of life for those affected by SERKAL syndrome.

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WNT4 Gene SERKAL Syndrome Genetic Test

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 WNT4 Gene SERKAL syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WNT4 Gene SERKAL syndrome NGS Genetic DNA Test gene WNT4

Test Details:

The WNT4 gene is responsible for providing instructions for making a protein called wingless-type MMTV integration site family member 4. This protein is involved in the development of various tissues and organs in the body, including the reproductive system and kidneys. SERKAL syndrome, also known as WNT4-related disorders, is a rare genetic condition caused by mutations in the WNT4 gene. This syndrome primarily affects the development of the kidneys and reproductive system in individuals assigned female at birth. It can lead to a variety of symptoms, including abnormal kidney function, genital abnormalities, and infertility.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the identification of genetic mutations and variants that may be associated with certain conditions or diseases. In the case of WNT4 gene-related disorders, NGS genetic testing can be used to detect mutations in the WNT4 gene, helping to confirm a diagnosis of SERKAL syndrome.

NGS genetic testing involves obtaining a DNA sample from the individual, typically through a blood sample or cheek swab. The DNA is then sequenced using advanced technology, allowing for the identification of any genetic variations or mutations in the WNT4 gene. The results of the test can help guide treatment decisions and provide valuable information for genetic counseling and family planning.

Test Name WNT4 Gene SERKAL syndrome 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 WNT4 Gene SERKAL syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WNT4 Gene SERKAL syndrome NGS Genetic DNA Test gene WNT4
Test Details

The WNT4 gene is responsible for providing instructions for making a protein called wingless-type MMTV integration site family member 4. This protein is involved in the development of various tissues and organs in the body, including the reproductive system and kidneys.

SERKAL syndrome, also known as WNT4-related disorders, is a rare genetic condition caused by mutations in the WNT4 gene. This syndrome primarily affects the development of the kidneys and reproductive system in individuals assigned female at birth. It can lead to a variety of symptoms, including abnormal kidney function, genital abnormalities, and infertility.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. It allows for the identification of genetic mutations and variants that may be associated with certain conditions or diseases. In the case of WNT4 gene-related disorders, NGS genetic testing can be used to detect mutations in the WNT4 gene, helping to confirm a diagnosis of SERKAL syndrome.

NGS genetic testing involves obtaining a DNA sample from the individual, typically through a blood sample or cheek swab. The DNA is then sequenced using advanced technology, allowing for the identification of any genetic variations or mutations in the WNT4 gene. The results of the test can help guide treatment decisions and provide valuable information for genetic counseling and family planning.