Abstract
Diagnosis of systemic autoinflammatory diseases (SAIDs) is often difficult to achieve and can delay the start of proper treatments and result in irreversible organ damage. In several patients with dominantly inherited SAID, postzygotic mutations have been detected as the disease-causing gene defects. Mutations with allele frequencies = 3% exceeds 99.9%. To date, we have detected three patients with mosaicism, two carrying likely pathogenic NLRP3 variants and one carrying a likely pathogenic TNFRSF1A variant with an allele frequency of 1.3%, confirming the relevance of the technology. The assay shown herein is a flexible, robust, fast, cost-effective, and highly reliable method for mosaicism detection; therefore, it is well suited for routine diagnostics.
Original language | English |
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Pages (from-to) | 943-950 |
Number of pages | 8 |
Journal | Journal of Molecular Diagnostics |
Volume | 21 |
Issue number | 6 |
DOIs | |
Publication status | Published - Nov-2019 |
Keywords
- SOMATIC MOSAICISM
- PERIODIC SYNDROME
- MUTATIONS
- RECEPTOR
- FEVER
- CIAS1