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ORC1 Gene Meier-Gorlin Syndrome Type 1 Genetic Test Cost

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

-21%

The ORC1 Gene Meier-Gorlin Syndrome Type 1 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the ORC1 gene, which are linked to Meier-Gorlin Syndrome Type 1. This rare genetic disorder is characterized by growth delays before and after birth, small ears, and, in many cases, absent or underdeveloped kneecaps. The test plays a crucial role in the early diagnosis and management of the syndrome, allowing for tailored care and interventions to improve the quality of life for affected individuals. Priced at 4400 AED, the test involves analyzing the patient’s DNA to detect any abnormalities in the ORC1 gene, providing a definitive diagnosis for families seeking answers to their medical concerns. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test is a vital resource for individuals and families affected by Meier-Gorlin Syndrome Type 1, offering hope and guidance through precise genetic insights.

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ORC1 Gene Meier-Gorlin Syndrome Type 1 Genetic Test

At DNA Labs UAE, we offer the ORC1 Gene Meier-Gorlin Syndrome Type 1 Genetic Test. This test is designed to identify genetic variations or mutations in the ORC1 gene, which is associated with Meier-Gorlin Syndrome Type 1.

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

Before undergoing the ORC1 Gene Meier-Gorlin 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 the disorder.

Test Details

Meier-Gorlin Syndrome Type 1 is a rare genetic disorder characterized by short stature, small ears, and small patellae (kneecaps). The ORC1 gene is associated with this syndrome. Our NGS genetic testing technique allows us to analyze multiple genes simultaneously, specifically sequencing the ORC1 gene to identify any variations or mutations that may be causing the disorder.

By undergoing the ORC1 Gene Meier-Gorlin Syndrome Type 1 Genetic Test, a diagnosis can be confirmed, providing valuable information for genetic counseling, family planning, and potential treatment options. This test is typically performed by a geneticist or genetic testing laboratory.

Test Name ORC1 Gene Meier-Gorlin 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 ORC1 Gene Meier-Gorlin syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ORC1 Gene Meier-Gorlin syndrome type 1 NGS Genetic DNA Test gene ORC1
Test Details

The ORC1 gene is associated with Meier-Gorlin syndrome type 1, a rare genetic disorder characterized by short stature, small ears, and small patellae (kneecaps).

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously to identify genetic variations or mutations. In the context of Meier-Gorlin syndrome type 1, an NGS genetic test would involve sequencing the ORC1 gene to identify any variations or mutations that may be causing the disorder.

This type of genetic testing can help confirm a diagnosis of Meier-Gorlin syndrome type 1 and provide valuable information for genetic counseling, family planning, and potential treatment options. It is typically performed by a geneticist or genetic testing laboratory.

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