Frontal lobe intra-axial schwannoma harboring a CHD7::VGLL3 fusion and heterozygous TSC2 p.F1510del mutation in a young child
We present a frontal lobe intra-axial parenchymal schwannoma containing a CHD7::VGLL3 gene fusion presenting in a 19 month-old male, the youngest patient yet reported for this lesion.
Authors
- Norman L. Lehman (ORCID: https://orcid.org/0000-0001-8394-2607)
- Anthony V. Nguyen (ORCID: https://orcid.org/0000-0002-3566-2659)
- Samuel Gearhart (ORCID: https://orcid.org/0000-0001-6095-7814)
- Eduardo Castro‐Echeverry
- Zied Abdullaev (ORCID: https://orcid.org/0000-0001-6345-2088)
- Eric R. Trumble
- Kenneth Aldape (ORCID: https://orcid.org/0000-0001-5119-7550)
- B. Berger
Institutions
- Baylor College of Medicine (US)
- Baylor Scott & White Medical Center - Temple (US)
- National Cancer Institute (US)
- Center for Cancer Research (US)
Publication Details
- Journal
- Molecular Biology Reports
- Published
- 2025-01-10
- DOI
- https://doi.org/10.1007/s11033-024-10201-8
- Primary Topic
- Hippo pathway signaling and YAP/TAZ
- Type
- article
- Field-Weighted Citation Impact
- 0.00