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NAA10 Gene Ogden Syndrome Genetic Test Cost

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

-21%

The NAA10 Gene Ogden Syndrome Genetic Test is a specific diagnostic tool offered by DNA Labs UAE, aimed at identifying mutations in the NAA10 gene, which are linked to Ogden Syndrome. This rare, X-linked genetic disorder primarily affects males and is characterized by developmental delays, intellectual disabilities, cardiac anomalies, and distinct facial features. The test, costing 4400 AED, involves analyzing the patient’s DNA to detect any abnormalities in the NAA10 gene, providing crucial information for diagnosis, management, and genetic counseling. By pinpointing the exact genetic mutation, healthcare providers can better understand the condition’s implications for the affected individual and their family, enabling personalized treatment plans and support strategies.

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NAA10 Gene Ogden Syndrome Genetic Test

Welcome to DNA Labs UAE, a leading genetic laboratory offering the NAA10 Gene Ogden Syndrome Genetic Test. In this blog, we will discuss the symptoms, diagnosis, and cost of this test, as well as provide detailed information about the NAA10 gene and Ogden syndrome.

Test Details

The NAA10 gene is responsible for encoding the N-alpha-acetyltransferase 10 protein. Mutations in this gene can lead to a rare genetic disorder called Ogden syndrome. Ogden syndrome is characterized by severe intellectual disability, delayed development, hypotonia (low muscle tone), and craniofacial abnormalities. Other common features include cardiac defects, seizures, and a shortened lifespan, with most affected individuals not surviving beyond infancy or early childhood.

Test Name

NAA10 Gene Ogden Syndrome 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

Prior to undergoing the NAA10 Gene Ogden Syndrome 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 with Ogden syndrome. This will help in identifying other family members at risk of being carriers or affected by the syndrome.

Test Benefits

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. It uses high-throughput sequencing technology to rapidly and accurately sequence DNA. NGS genetic testing can be used to identify mutations in the NAA10 gene and confirm a diagnosis of Ogden syndrome. By identifying the specific genetic mutation causing Ogden syndrome, NGS genetic testing can provide valuable information for clinical management, genetic counseling, and potential future treatment options.

Conclusion

The NAA10 Gene Ogden Syndrome Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing Ogden syndrome. With its comprehensive analysis and accurate results, this test can help in understanding the inheritance pattern of the condition and identifying other family members at risk. The cost of the test is 4400.0 AED, and the sample can be either blood or extracted DNA. The report will be delivered within 3 to 4 weeks. If you suspect Ogden syndrome or have a family history of the condition, consult a pediatrician and consider undergoing this genetic test for a better understanding and management of the syndrome.

Test Name NAA10 Gene Ogden syndrome 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 NAA10 Gene Ogden syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NAA10 Gene Ogden syndrome NGS Genetic DNA Test gene NAA10
Test Details

The NAA10 gene is responsible for encoding the N-alpha-acetyltransferase 10 protein. Mutations in this gene can lead to a rare genetic disorder called Ogden syndrome.

Ogden syndrome is characterized by severe intellectual disability, delayed development, hypotonia (low muscle tone), and craniofacial abnormalities. Other common features include cardiac defects, seizures, and a shortened lifespan, with most affected individuals not surviving beyond infancy or early childhood.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. It uses high-throughput sequencing technology to rapidly and accurately sequence DNA. NGS genetic testing can be used to identify mutations in the NAA10 gene and confirm a diagnosis of Ogden syndrome.

By identifying the specific genetic mutation causing Ogden syndrome, NGS genetic testing can provide valuable information for clinical management, genetic counseling, and potential future treatment options. It can also help in understanding the inheritance pattern of the condition and identifying other family members at risk of being carriers or affected by the syndrome.

SKU: TEST-4287 Category:

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