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TTC21B Gene Short-Rib Thoracic Dysplasia Type 4 with or Without Polydactyly Genetic Test Cost

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

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The TTC21B Gene Short-Rib Thoracic Dysplasia Type 4 with or Without Polydactyly Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE. This test is designed to identify mutations in the TTC21B gene, which are known to cause Short-Rib Thoracic Dysplasia Type 4 (SRTD4). This condition is characterized by the development of a narrow chest, short ribs, shortened bones in the arms and legs, and potentially, additional fingers or toes (polydactyly). The test plays a crucial role in the early diagnosis and management of the disorder, allowing for appropriate medical interventions and genetic counseling for affected families. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and expert interpretation provided by DNA Labs UAE to ensure accurate results.

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TTC21B Gene Short-rib thoracic dysplasia type 4 with or without polydactyly Genetic Test

At DNA Labs UAE, we offer the TTC21B Gene Short-rib thoracic dysplasia type 4 with or without polydactyly Genetic Test at a cost of AED 4400.0. This test is used to diagnose individuals with the genetic disorder known as short-rib thoracic dysplasia type 4 with or without polydactyly (SRTD4).

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

Before undergoing the TTC21B Gene Short-rib thoracic dysplasia type 4 with or without polydactyly NGS Genetic DNA 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 by the disorder.

Test Details

The TTC21B gene is associated with short-rib thoracic dysplasia type 4 with or without polydactyly (SRTD4). This genetic disorder is characterized by skeletal abnormalities, including a narrow thorax, short ribs, and shortening of the long bones. It may also involve polydactyly, which is the presence of extra fingers or toes.

NGS (Next-Generation Sequencing) genetic testing is used to analyze the DNA sequence of multiple genes simultaneously. In the case of SRTD4, NGS can identify mutations or variations in the TTC21B gene that may be causing the disorder. By performing this genetic test, healthcare professionals can provide a definitive diagnosis for individuals suspected of having SRTD4. This can help guide medical management, provide accurate genetic counseling, and potentially offer targeted treatment options or interventions for affected individuals.

Test Name TTC21B Gene Short-rib thoracic dysplasia type 4 with or without polydactyly 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 TTC21B Gene Short-rib thoracic dysplasia type 4 with or without polydactyly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TTC21B Gene Short-rib thoracic dysplasia type 4 with or without polydactyly NGS Genetic DNA Test gene TTC21B
Test Details

The TTC21B gene is associated with a genetic disorder called short-rib thoracic dysplasia type 4 with or without polydactyly (SRTD4). This disorder is characterized by skeletal abnormalities, including a narrow thorax, short ribs, and shortening of the long bones. It may also involve polydactyly, which is the presence of extra fingers or toes.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of multiple genes simultaneously. In the case of SRTD4, NGS can be used to identify mutations or variations in the TTC21B gene that may be causing the disorder.

By performing this genetic test, healthcare professionals can provide a definitive diagnosis for individuals suspected of having SRTD4. This can help guide medical management, provide accurate genetic counseling, and potentially offer targeted treatment options or interventions for affected individuals.

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