RAB23 Gene Carpenter Syndrome Genetic Test sale cost 3200 AED
UPB1 Gene Beta-Ureidopropionase Deficiency Genetic Test sale cost 4400 AED UPB1 Gene Beta-Ureidopropionase Deficiency Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
MECP2 Gene Central Hypoventilation Syndrome Congenital Genetic Test sale cost 4400 AED MECP2 Gene Central Hypoventilation Syndrome Congenital Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

RAB23 Gene Carpenter Syndrome Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 3,200 د.إ.

-43%

The RAB23 gene plays a critical role in the development of Carpenter syndrome, a rare genetic disorder characterized by abnormalities in the skull, fingers, toes, and obesity, among other symptoms. The Carpenter Syndrome Genetic Test, specifically targeting the RAB23 gene, is a crucial diagnostic tool available at DNA Labs UAE. This test helps in the early detection and confirmation of Carpenter syndrome, facilitating timely intervention and management of the condition. Priced at 3200 AED, the test involves analyzing the patient’s DNA to identify mutations in the RAB23 gene, which are indicative of the syndrome. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test is a step forward in personalized medicine, offering hope and options for affected families.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

RAB23 Gene Carpenter Syndrome Genetic Test

Test Details

The RAB23 gene is associated with Carpenter syndrome, a rare genetic disorder characterized by craniofacial and skeletal abnormalities. This genetic test uses NGS (Next-Generation Sequencing) technology to analyze the RAB23 gene for mutations or variations that may be responsible for the disorder.

Test Components

  • Price: 3200.0 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

Prior to undergoing the RAB23 Gene Carpenter Syndrome NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the disorder.

Benefits of NGS Genetic Testing

NGS genetic testing allows for a more comprehensive and efficient analysis of multiple genes compared to traditional genetic testing methods. In the context of Carpenter syndrome, NGS genetic testing can provide valuable information about the presence of mutations in the RAB23 gene, aiding in diagnosis, genetic counseling, and potential treatment options.

Consultation

It is important to consult with a genetic counselor or healthcare provider to discuss the benefits, limitations, and potential risks associated with NGS genetic testing for Carpenter syndrome or any other genetic disorder.

Test Name RAB23 Gene Carpenter syndrome Genetic Test
Components
Price 3200.0 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 RAB23 Gene Carpenter syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAB23 Gene Carpenter syndrome NGS Genetic DNA Test gene RAB23
Test Details

The RAB23 gene is associated with Carpenter syndrome, which is a rare genetic disorder characterized by craniofacial abnormalities, such as a high forehead, wide-set eyes, and a flat nasal bridge, as well as other skeletal abnormalities, such as fused or missing fingers and toes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Carpenter syndrome, NGS genetic testing can be used to identify mutations or variations in the RAB23 gene that may be responsible for the disorder.

By analyzing the patient’s DNA, NGS genetic testing can provide valuable information about the presence of mutations in the RAB23 gene, which can help with diagnosis, genetic counseling, and potential treatment options. It allows for a more comprehensive and efficient analysis of multiple genes, compared to traditional genetic testing methods.

It is important to consult with a genetic counselor or healthcare provider to discuss the benefits, limitations, and potential risks associated with NGS genetic testing for Carpenter syndrome or any other genetic disorder.

SKU: TEST-4025 Category:

Related products