An estimation of global genetic prevalence of PLA2G6-associated neurodegeneration
Our estimates highlight the significant underdiagnosis of PLA2G6-associated neurodegeneration and underscores the need for increased awareness and diagnostic efforts. Furthermore, our study revealed a higher carrier frequency of PLA2G6 variants in African and Asian populations, stressing the importance of expanded genetic sequencing in non-European populations to ensure accurate and comprehensive diagnosis. Future research should focus on confirming our findings and implementing expanded sequencing strategies to facilitate maximal and accurate diagnosis, particularly in non-European populations.
Authors
- Amina Kurtović-Kozarić (ORCID: https://orcid.org/0000-0002-6063-7260)
- Jordan C. Wood
- Samantha Baxter (ORCID: https://orcid.org/0000-0003-4616-9234)
- Moriel Singer‐Berk (ORCID: https://orcid.org/0000-0001-8148-0648)
- Amanda Hope
- Emily Evangelista (ORCID: https://orcid.org/0000-0002-1018-7310)
- Leena Panwala
- Mark J. Kiel (ORCID: https://orcid.org/0000-0003-0931-1983)
- Stefanie M. Heinrich
Institutions
- Broad Institute (US)
- Center for Genomic Science (IT)
Publication Details
- Journal
- Orphanet Journal of Rare Diseases
- Published
- 2024-10-18
- DOI
- https://doi.org/10.1186/s13023-024-03275-x
- Citations
- 8
- Primary Topic
- Neurological diseases and metabolism
- Type
- article
- Field-Weighted Citation Impact
- 1.98