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NPR2 Gene Acromesomelic Dysplasia Maroteaux Type Genetic Test Cost

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

-43%

The NPR2 gene acromesomelic dysplasia Maroteaux type genetic test is a specialized diagnostic procedure aimed at identifying mutations in the NPR2 gene, which are responsible for causing acromesomelic dysplasia Maroteaux type (AMDM). AMDM is a rare genetic disorder characterized by severe shortening of the bones in the arms and legs, among other skeletal abnormalities. The test involves analyzing the patient’s DNA to detect any genetic alterations in the NPR2 gene that could lead to the condition.

This genetic test is crucial for accurate diagnosis, allowing for appropriate management and counseling for affected individuals and their families. It can also provide valuable information for prospective parents with a family history of AMDM, helping them understand their risks of passing the condition to their offspring.

The test is available at DNA Labs UAE, a leading facility in genetic testing and diagnostics. The cost of the test is set at 3200 AED. Given the complexity of genetic testing and the specialized analysis required, this price reflects the comprehensive service provided, including the expertise of the laboratory technicians and genetic counselors who may be involved in interpreting the results.

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NPR2 Gene Acromesomelic Dysplasia Maroteaux Type Genetic Test

At DNA Labs UAE, we offer the NPR2 Gene Acromesomelic Dysplasia Maroteaux Type Genetic Test at a cost of AED 3200.0.

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

Before undergoing the NPR2 Gene Acromesomelic Dysplasia Maroteaux Type 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 NPR2 Gene Acromesomelic Dysplasia Maroteaux Type NGS Genetic DNA Test gene NPR2.

Test Details

The NPR2 gene is associated with a rare genetic disorder called acromesomelic dysplasia, Maroteaux type. This disorder affects the development of bones in the limbs and results in short stature and skeletal abnormalities.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the DNA sequence of the NPR2 gene and identify any mutations or variations that may be present. This type of testing can help in confirming a diagnosis of acromesomelic dysplasia, Maroteaux type and determining the specific genetic cause of the disorder.

NGS genetic testing involves sequencing large amounts of DNA in a high-throughput manner, allowing for the analysis of multiple genes simultaneously. This can provide a comprehensive view of the genetic variations in the NPR2 gene and other relevant genes that may be associated with the disorder.

By identifying the specific genetic mutation or variation in the NPR2 gene, NGS testing can help in understanding the underlying cause of acromesomelic dysplasia, Maroteaux type. This information can be useful for genetic counseling, family planning, and potentially guiding treatment options or interventions for individuals affected by this disorder.

Test Name NPR2 Gene Acromesomelic dysplasia Maroteaux type 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 NPR2 Gene Acromesomelic dysplasia, Maroteaux type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NPR2 Gene Acromesomelic dysplasia, Maroteaux type NGS Genetic DNA Test gene NPR2
Test Details

The NPR2 gene is associated with a rare genetic disorder called acromesomelic dysplasia, Maroteaux type. This disorder affects the development of bones in the limbs and results in short stature and skeletal abnormalities.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the DNA sequence of the NPR2 gene and identify any mutations or variations that may be present. This type of testing can help in confirming a diagnosis of acromesomelic dysplasia, Maroteaux type and determining the specific genetic cause of the disorder.

NGS genetic testing involves sequencing large amounts of DNA in a high-throughput manner, allowing for the analysis of multiple genes simultaneously. This can provide a comprehensive view of the genetic variations in the NPR2 gene and other relevant genes that may be associated with the disorder.

By identifying the specific genetic mutation or variation in the NPR2 gene, NGS testing can help in understanding the underlying cause of acromesomelic dysplasia, Maroteaux type. This information can be useful for genetic counseling, family planning, and potentially guiding treatment options or interventions for individuals affected by this disorder.

SKU: TEST-3974 Category:

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