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CUL7 Gene Three M Syndrome Type 1 Genetic Test Cost

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

-21%

The CUL7 gene Three M Syndrome Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE. Priced at 4400 AED, this test is designed to identify mutations in the CUL7 gene, which are associated with Three M Syndrome Type 1. Three M Syndrome is a rare genetic condition characterized by growth retardation, distinctive facial features, and skeletal abnormalities. The CUL7 gene plays a crucial role in the regulation of cell division and growth, and mutations in this gene can lead to the development of this syndrome.

The test involves the collection of a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities in the CUL7 gene. By identifying these mutations, the test can confirm a diagnosis of Three M Syndrome Type 1, allowing for early intervention and management of the condition. DNA Labs UAE provides this testing service with the aim of offering accurate genetic diagnosis and supporting individuals and families in understanding their genetic health.

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  • This test is not intended for medical diagnosis or treatment
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CUL7 Gene Three M syndrome type 1 Genetic Test

Components:

  • Test Name: CUL7 Gene Three M 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:

Clinical History of Patient who is going for CUL7 Gene Three M syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CUL7 Gene Three M syndrome type 1 NGS Genetic DNA Test gene CUL7.

Test Details:

The CUL7 gene is associated with Three M syndrome type 1, which is a rare genetic disorder characterized by short stature, facial dysmorphism, and skeletal abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes to identify any variations or mutations that may be associated with a particular genetic disorder, such as Three M syndrome type 1. This test can help confirm a diagnosis, provide information about the specific genetic cause of the disorder, and guide treatment and management options.

Test Name CUL7 Gene Three M 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 CUL7 Gene Three M syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CUL7 Gene Three M syndrome type 1 NGS Genetic DNA Test gene CUL7
Test Details

The CUL7 gene is associated with Three M syndrome type 1, which is a rare genetic disorder characterized by short stature, facial dysmorphism, and skeletal abnormalities. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of a person’s genes to identify any variations or mutations that may be associated with a particular genetic disorder, such as Three M syndrome type 1. This test can help confirm a diagnosis, provide information about the specific genetic cause of the disorder, and guide treatment and management options.