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HPSE2 Gene Urofacial Syndrome Type 1 Genetic Test Cost

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

-21%

The HPSE2 Gene Urofacial Syndrome Type 1 Genetic Test is a specialized diagnostic tool designed to identify mutations in the HPSE2 gene, which are associated with Urofacial Syndrome Type 1 (UFS1). This condition, also known as Ochoa syndrome, is a rare genetic disorder characterized by an abnormal facial expression and difficulties with urinary tract function. Symptoms often include a distinctive facial grimace when attempting to smile and various degrees of urinary tract problems, which can lead to serious kidney damage if left untreated.

The test, available at DNA Labs UAE, is crucial for the early detection and management of UFS1. It involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific genetic mutations in the HPSE2 gene. Identifying these mutations can confirm a diagnosis of Urofacial Syndrome Type 1, allowing for appropriate medical interventions and genetic counseling for affected families.

The cost of the HPSE2 Gene Urofacial Syndrome Type 1 Genetic Test at DNA Labs UAE is 4400 AED. This investment can be invaluable for families seeking answers to unexplained urinary and facial symptoms in their loved ones, paving the way for targeted treatments and improved quality of life for individuals with UFS1.

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HPSE2 Gene Urofacial Syndrome Type 1 Genetic Test

Welcome to DNA Labs UAE, where we offer the HPSE2 Gene Urofacial Syndrome Type 1 Genetic Test. This test helps in diagnosing and understanding Urofacial Syndrome Type 1, also known as Ochoa Syndrome. Read on to learn more about the test details, components, price, and more.

Test Components

  • Test Name: HPSE2 Gene Urofacial 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Before undergoing the HPSE2 Gene Urofacial Syndrome Type 1 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 Urofacial Syndrome Type 1. This will help in understanding the genetic basis of the condition and guide the testing process.

Test Details

The HPSE2 gene is associated with Urofacial Syndrome Type 1, also known as Ochoa Syndrome. This syndrome is characterized by urinary tract dysfunction and abnormal facial expressions. To identify mutations or variations in the HPSE2 gene responsible for the syndrome, we use NGS (Next-Generation Sequencing) technology. NGS allows for the analysis of multiple genes simultaneously.

During the NGS genetic testing process, the DNA of the individual suspected to have Urofacial Syndrome Type 1 is extracted from a blood or saliva sample. This DNA sample is then sent to our specialized laboratory for analysis. Our laboratory will sequence the DNA to detect any changes or mutations in the HPSE2 gene. The results of the NGS genetic test will provide valuable information for healthcare professionals to diagnose the condition, predict the risk of developing the syndrome, and guide treatment decisions.

If you suspect that you or a family member may have Urofacial Syndrome Type 1, we recommend undergoing the HPSE2 Gene Urofacial Syndrome Type 1 Genetic Test. Our expert team at DNA Labs UAE is dedicated to providing accurate and reliable genetic testing services to help improve the lives of individuals affected by genetic disorders.

Test Name HPSE2 Gene Urofacial 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for HPSE2 Gene Urofacial syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HPSE2 Gene Urofacial syndrome type 1 NGS Genetic DNA Test gene HPSE2
Test Details

The HPSE2 gene is associated with Urofacial syndrome type 1, also known as Ochoa syndrome. This syndrome is characterized by urinary tract dysfunction and abnormal facial expressions.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the analysis of multiple genes simultaneously. In the context of Urofacial syndrome type 1, NGS genetic testing can be used to identify mutations or variations in the HPSE2 gene that may be responsible for the syndrome.

NGS genetic testing involves sequencing the DNA of an individual to detect any changes or mutations in specific genes of interest. This can help in diagnosing the condition, predicting the risk of developing the syndrome, and guiding treatment decisions.

If a person is suspected to have Urofacial syndrome type 1, their DNA can be extracted from a blood or saliva sample and sent to a specialized laboratory for NGS genetic testing. The laboratory will analyze the HPSE2 gene for any mutations or variations that may be associated with the syndrome.

The results of the NGS genetic test can provide valuable information for healthcare professionals to better understand the genetic basis of Urofacial syndrome type 1 and develop personalized treatment plans for affected individuals.

SKU: TEST-4425 Category:

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