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LFNG Gene Spondylocostal Dysostosis Autosomal Recessive Type 3 Genetic Test

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

-21%

The LFNG Gene Spondylocostal Dysostosis Autosomal Recessive Type 3 Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the LFNG gene, which are associated with Spondylocostal Dysostosis, Autosomal Recessive Type 3 (SCDO3). This condition is characterized by abnormal development of the vertebrae and ribs, leading to a shortened trunk, scoliosis, and other skeletal abnormalities. The test is crucial for early diagnosis, allowing for appropriate management and genetic counseling for affected families.

Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing the genetic material for specific mutations in the LFNG gene. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic alterations associated with SCDO3.

By opting for this genetic test, individuals with a family history of Spondylocostal Dysostosis or related symptoms can gain valuable insights into their genetic makeup, enabling informed decisions about their health and future.

Description

LFNG Gene Spondylocostal dysostosis autosomal recessive type 3 Genetic Test

Components: LFNG Gene Spondylocostal dysostosis autosomal recessive type 3 Genetic Test

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: Osteology Dermatology Immunology Disorders

Doctor: Dermatologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for LFNG Gene Spondylocostal dysostosis, autosomal recessive type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LFNG Gene Spondylocostal dysostosis, autosomal recessive type 3 NGS Genetic DNA Test gene LFNG

Test Details: LFNG gene spondylocostal dysostosis, autosomal recessive type 3 NGS genetic test is a type of genetic test that analyzes the LFNG gene for mutations associated with spondylocostal dysostosis. Spondylocostal dysostosis is a rare genetic disorder characterized by abnormal vertebral segmentation and rib abnormalities. NGS (Next-Generation Sequencing) technology is used in this test to analyze the entire coding region of the LFNG gene, which is responsible for producing a protein involved in vertebral and rib development. The test can identify various types of mutations in the LFNG gene, including point mutations, small insertions or deletions, and larger structural rearrangements. This genetic test is performed on a DNA sample, typically obtained through a blood sample or cheek swab. The sample is then analyzed in a laboratory using NGS technology to identify any mutations or variations in the LFNG gene. The results of the test can help confirm a diagnosis of spondylocostal dysostosis and determine the specific genetic cause of the condition. This information can be used to guide patient management, provide genetic counseling to affected individuals and their families, and potentially inform reproductive decisions. It is important to note that this genetic test specifically focuses on autosomal recessive type 3 spondylocostal dysostosis caused by mutations in the LFNG gene. There are other types of spondylocostal dysostosis caused by mutations in different genes, and separate genetic tests may be required to diagnose those specific types.

Test Name	LFNG Gene Spondylocostal dysostosis autosomal recessive type 3 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	Osteology Dermatology Immunology Disorders
Doctor	Dermatologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for LFNG Gene Spondylocostal dysostosis, autosomal recessive type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LFNG Gene Spondylocostal dysostosis, autosomal recessive type 3 NGS Genetic DNA Test gene LFNG
Test Details	LFNG gene spondylocostal dysostosis, autosomal recessive type 3 NGS genetic test is a type of genetic test that analyzes the LFNG gene for mutations associated with spondylocostal dysostosis. Spondylocostal dysostosis is a rare genetic disorder characterized by abnormal vertebral segmentation and rib abnormalities. NGS (Next-Generation Sequencing) technology is used in this test to analyze the entire coding region of the LFNG gene, which is responsible for producing a protein involved in vertebral and rib development. The test can identify various types of mutations in the LFNG gene, including point mutations, small insertions or deletions, and larger structural rearrangements. This genetic test is performed on a DNA sample, typically obtained through a blood sample or cheek swab. The sample is then analyzed in a laboratory using NGS technology to identify any mutations or variations in the LFNG gene. The results of the test can help confirm a diagnosis of spondylocostal dysostosis and determine the specific genetic cause of the condition. This information can be used to guide patient management, provide genetic counseling to affected individuals and their families, and potentially inform reproductive decisions. It is important to note that this genetic test specifically focuses on autosomal recessive type 3 spondylocostal dysostosis caused by mutations in the LFNG gene. There are other types of spondylocostal dysostosis caused by mutations in different genes, and separate genetic tests may be required to diagnose those specific types.