Symptoms and Testing information for Sphingo Enzyme Panel NGS Genetic Test

Symptoms and Testing information for Sphingo Enzyme Panel NGS Genetic Test

In the realm of genetic testing, the Sphingo Enzyme Panel NGS Genetic Test stands out as a pivotal tool for diagnosing a range of disorders related to sphingolipid metabolism. These disorders, often severe and progressive, can significantly impact an individual’s quality of life. Conducted by DNA Labs UAE, a leading institution in genetic diagnostics, this test offers a comprehensive analysis to detect genetic mutations associated with sphingolipidoses. Understanding the symptoms that prompt this genetic testing and the associated costs is crucial for patients and healthcare providers alike.

Understanding Sphingolipidoses

Sphingolipidoses are a group of metabolic disorders caused by the malfunction of sphingolipid metabolism. These disorders result from inherited mutations that affect the enzymes responsible for breaking down sphingolipids in the body. When these enzymes are deficient or malfunctioning, sphingolipids accumulate in various tissues, leading to a range of symptoms. The Sphingo Enzyme Panel NGS Genetic Test is designed to detect mutations in genes responsible for these enzymes, offering a pathway to accurate diagnosis and tailored treatment.

Indications for the Sphingo Enzyme Panel NGS Genetic Test

The decision to undergo the Sphingo Enzyme Panel NGS Genetic Test is often prompted by the presence of specific symptoms indicative of sphingolipidoses. These symptoms vary widely depending on the specific disorder and the organs affected. However, common symptoms that may suggest the need for genetic testing include:

  • Developmental delay or regression
  • Seizures
  • Motor dysfunction
  • Visual impairment or blindness
  • Hearing loss
  • Enlarged liver and spleen (hepatosplenomegaly)
  • Skeletal abnormalities
  • Cherry red spot on the macula
  • Neurological decline

It is essential for healthcare providers to recognize these symptoms early, as a timely diagnosis can significantly influence the management and outcome of these disorders.

Cost of the Test

The cost of the Sphingo Enzyme Panel NGS Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis necessary to identify the genetic mutations responsible for sphingolipidoses. While the cost may seem significant, it is crucial to consider the value of a precise diagnosis in guiding effective treatment and management strategies for affected individuals.

Why Choose DNA Labs UAE?

DNA Labs UAE is at the forefront of genetic testing, offering a wide range of services to diagnose genetic conditions accurately. The Sphingo Enzyme Panel NGS Genetic Test is conducted by experienced professionals using state-of-the-art technology to ensure reliable results. By choosing DNA Labs UAE, patients gain access to expert guidance, support, and the latest in genetic diagnostic techniques.


The Sphingo Enzyme Panel NGS Genetic Test is a critical tool in diagnosing sphingolipidoses, offering hope to individuals and families affected by these challenging conditions. Recognizing the symptoms that warrant this genetic testing is the first step towards obtaining a diagnosis and embarking on the path to tailored treatment. With the expertise of DNA Labs UAE and the comprehensive analysis provided by this test, patients have access to the highest standard of care in genetic diagnostics. For more information on the Sphingo Enzyme Panel NGS Genetic Test, visit DNA Labs UAE.

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