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NEK1 Gene Short-Rib Thoracic Dysplasia Type 6 with or Without Polydactyly Genetic Test Cost

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

-21%

The NEK1 Gene Short-Rib Thoracic Dysplasia Type 6 with or Without Polydactyly Genetic Test is a specialized diagnostic examination conducted to identify mutations in the NEK1 gene, which are linked to the development of Short-Rib Thoracic Dysplasia Type 6. This condition is characterized by a narrow chest, short ribs, shortened bones in the arms and legs, and potentially, extra fingers or toes (polydactyly). Identifying mutations in the NEK1 gene is crucial for accurate diagnosis, informing treatment options, and understanding the risk of passing the condition to future generations.

DNA Labs UAE offers this comprehensive genetic test at a cost of 4400 AED. The test is performed using advanced genomic technologies to ensure high accuracy and reliability. By choosing DNA Labs UAE for this genetic testing, patients and healthcare providers can expect professional service, confidentiality, and support throughout the testing process. This test is an invaluable tool for families seeking answers about this rare skeletal dysplasia, providing them with the necessary information to make informed health and family planning decisions.

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NEK1 Gene Short-rib thoracic dysplasia type 6 with or without polydactyly Genetic Test

Test Name: NEK1 Gene Short-rib thoracic dysplasia type 6 with or without polydactyly Genetic Test

Components: NGS Technology

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 NEK1 Gene Short-rib thoracic dysplasia type 6 with or without polydactyly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NEK1 Gene Short-rib thoracic dysplasia type 6 with or without polydactyly NGS Genetic DNA Test gene NEK1

Test Details: The NEK1 gene is associated with a genetic disorder called short-rib thoracic dysplasia type 6 with or without polydactyly (SRTD6). This disorder is characterized by abnormal development of the ribs and bones in the thorax, resulting in a narrow and shortened chest. It can also be associated with extra fingers or toes (polydactyly).

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of SRTD6, NGS testing can be used to analyze the NEK1 gene for any disease-causing mutations or variations. By identifying specific mutations or variations in the NEK1 gene, NGS testing can help confirm a diagnosis of SRTD6 and provide information about the genetic basis of the condition. This information can be helpful for medical management, genetic counseling, and family planning.

Test Name NEK1 Gene Short-rib thoracic dysplasia type 6 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 NEK1 Gene Short-rib thoracic dysplasia type 6 with or without polydactyly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NEK1 Gene Short-rib thoracic dysplasia type 6 with or without polydactyly NGS Genetic DNA Test gene NEK1
Test Details

The NEK1 gene is associated with a genetic disorder called short-rib thoracic dysplasia type 6 with or without polydactyly (SRTD6). This disorder is characterized by abnormal development of the ribs and bones in the thorax, resulting in a narrow and shortened chest. It can also be associated with extra fingers or toes (polydactyly).

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously. In the case of SRTD6, NGS testing can be used to analyze the NEK1 gene for any disease-causing mutations or variations.

By identifying specific mutations or variations in the NEK1 gene, NGS testing can help confirm a diagnosis of SRTD6 and provide information about the genetic basis of the condition. This information can be helpful for medical management, genetic counseling, and family planning.

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