SMN1 Gene Spinal Muscular Atrophy Type 1 Genetic Test sale cost 4400 AED
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SMN1 Gene Spinal Muscular Atrophy Type 1 Genetic Test Cost

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

-21%

The SMN1 Gene Spinal Muscular Atrophy Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the SMN1 gene, which are indicative of Spinal Muscular Atrophy (SMA) Type 1. SMA Type 1, also known as Werdnig-Hoffmann disease, is a severe form of spinal muscular atrophy that manifests in infancy and is characterized by muscle weakness and atrophy resulting from the degeneration of motor neurons in the spinal cord. The test is crucial for early diagnosis and management of the condition, allowing for timely intervention and support for affected individuals and their families. Priced at 4400 AED, this genetic test provides a valuable tool for clinicians and genetic counselors in the assessment and understanding of this genetic disorder, paving the way for personalized treatment plans and improved patient outcomes.

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Test Name SMN1 Gene Spinal muscular atrophy type 1 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SMN1 Gene Spinal muscular atrophy type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SMN1 Gene Spinal muscular atrophy type 1
Test Details

The SMN1 gene is associated with spinal muscular atrophy (SMA) type 1, which is a genetic disorder that affects the muscles and motor neurons. SMA type 1 is the most severe form of the condition and typically manifests in infancy.

NGS (Next-Generation Sequencing) is a high-throughput sequencing technology that can analyze multiple genes simultaneously. In the context of genetic testing for SMA type 1, NGS can be used to identify mutations or variations in the SMN1 gene that are associated with the condition.

The NGS genetic test for SMA type 1 involves obtaining a DNA sample, usually through a blood or saliva sample, and sequencing the SMN1 gene using NGS technology. The test can detect specific mutations or variations in the gene that are known to cause SMA type 1.

The results of the NGS genetic test can help diagnose SMA type 1 and determine the specific genetic cause of the condition. This information is important for understanding the prognosis and potential treatment options for individuals with SMA type 1.

SKU: TEST-2040