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RBBP8 Gene Seckel Syndrome Type 2 Genetic Test Cost

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

-21%

The RBBP8 Gene Seckel Syndrome Type 2 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the RBBP8 gene, which are linked to Seckel Syndrome Type 2. Seckel Syndrome is a rare genetic disorder characterized by growth delays, microcephaly (unusually small head size), and a range of other developmental anomalies. The test plays a crucial role in the early detection and management of the condition, enabling healthcare professionals to devise appropriate treatment and care plans for affected individuals.

Priced at 4400 AED, the test involves collecting a DNA sample from the patient, usually through a blood draw or cheek swab, which is then analyzed in the state-of-the-art facilities of DNA Labs UAE. The laboratory employs cutting-edge genetic sequencing technologies to accurately identify mutations in the RBBP8 gene, offering insights into the patient’s condition and genetic makeup. This information is vital for families seeking to understand the genetic underpinnings of Seckel Syndrome Type 2, assess the risk of recurrence in future pregnancies, and explore potential therapeutic avenues.

Home  Sample collection service available

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  • This test is not intended for medical diagnosis or treatment
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RBBP8 Gene Seckel Syndrome Type 2 Genetic Test

Welcome to DNA Labs UAE, where we offer the RBBP8 Gene Seckel syndrome type 2 Genetic Test. This test is designed to help diagnose Seckel syndrome type 2, a rare genetic disorder characterized by growth retardation, microcephaly, and intellectual disability.

Test Details

The RBBP8 gene is associated with Seckel syndrome type 2. Our NGS (Next-Generation Sequencing) genetic testing method allows for the simultaneous analysis of multiple genes, including the RBBP8 gene. This technology uses high-throughput sequencing to efficiently sequence large amounts of DNA. By identifying mutations or variations in the RBBP8 gene, our test can help confirm a diagnosis of Seckel syndrome type 2.

Components and Price

  • Test Name: RBBP8 Gene Seckel syndrome type 2 Genetic Test
  • Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

Reports are typically delivered within 3 to 4 weeks.

Test Type and Doctor

  • Test Type: Dysmorphology
  • Doctor: Pediatrics

Test Department

Our Genetics department handles the RBBP8 Gene Seckel syndrome type 2 Genetic Test.

Pre Test Information

Prior to the test, we require a clinical history of the patient who will undergo the RBBP8 Gene Seckel syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session will also be conducted to draw a pedigree chart of family members affected by the RBBP8 gene.

Test Name RBBP8 Gene Seckel syndrome type 2 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 RBBP8 Gene Seckel syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RBBP8 Gene Seckel syndrome type 2 NGS Genetic DNA Test gene RBBP8
Test Details

The RBBP8 gene is associated with Seckel syndrome type 2, which is a rare genetic disorder characterized by growth retardation, microcephaly (small head size), and intellectual disability.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. It uses high-throughput sequencing technology to rapidly and efficiently sequence large amounts of DNA. NGS genetic testing can be used to identify mutations or variations in the RBBP8 gene, which can help confirm a diagnosis of Seckel syndrome type 2.

SKU: TEST-4357 Category:

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