Pseudodeficiency alleles: Difference between revisions
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Latest revision as of 00:05, 18 March 2025
Pseudodeficiency alleles are genetic variants that can cause a false positive result in newborn screening tests for certain metabolic disorders. These alleles do not cause disease symptoms, but they can interfere with the biochemical assays used in newborn screening, leading to a false diagnosis of a metabolic disorder.
Overview[edit]
Pseudodeficiency alleles are genetic variants that can cause a false positive result in newborn screening tests for certain metabolic disorders. These alleles do not cause disease symptoms, but they can interfere with the biochemical assays used in newborn screening, leading to a false diagnosis of a metabolic disorder.
Characteristics[edit]
Pseudodeficiency alleles are typically found in genes that encode enzymes involved in the metabolism of certain substances. These alleles can cause the enzyme to function less efficiently, leading to an accumulation of the substance in the body. However, this accumulation is not sufficient to cause disease symptoms.
Impact on Newborn Screening[edit]
Newborn screening tests are designed to detect metabolic disorders by measuring the levels of certain substances in the body. If a pseudodeficiency allele is present, the test may indicate a high level of the substance, leading to a false positive result. This can cause unnecessary stress and medical intervention for the family.
Examples[edit]
One example of a pseudodeficiency allele is found in the gene for the enzyme arylsulfatase A. This allele can cause a false positive result in newborn screening tests for metachromatic leukodystrophy, a severe metabolic disorder.
Another example is found in the gene for the enzyme galactocerebrosidase. This allele can cause a false positive result in newborn screening tests for Krabbe disease, another severe metabolic disorder.
Conclusion[edit]
While pseudodeficiency alleles can cause false positive results in newborn screening tests, they do not cause disease symptoms. Therefore, it is important for healthcare providers to confirm a positive screening result with additional diagnostic testing to avoid unnecessary medical intervention.


