BRAF V600E mutation associated with papillary high-grade serous ovarian cystadenocarcinoma in a 22q11.2DS patient
Objective: Ovarian cancers exhibit very heterogeneous genetic and genomic aberrations with various pathogenetic and prognostic values. Chromosome 22 abnormalities, including del(22q) and duplications, are genetic multisystemic disorders, most commonly affecting cardiovascular, immune, and gastrointe...
Saved in:
| Main Authors: | Maria Antonietta Castaldi, Nadia Petrillo, Carmine Selleri, Monica Ianniello, Anna Maria Della Corte, Eloisa Evangelista, Luigia De Falco, Roberto Sirica, Marika Casillo, Alessia Caleo, Alessandro Caputo, Pio Zeppa, Salvatore Giovanni Castaldi, Pasqualina Scala, Bianca Serio, Giovanni Savarese, Valentina Giudice |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2025-06-01
|
| Series: | Gynecologic Oncology Reports |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2352578925001018 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Understanding obesity in children with 22q11.2 deletion syndrome
by: Walter Maria Sarli, et al.
Published: (2025-07-01) -
A case-control study of bleeding risk in children with 22q11.2 deletion syndrome undergoing cardiac surgery
by: T. Blaine Crowley, et al.
Published: (2024-12-01) -
Drug-induced parkinsonism in a patient with DiGeorge syndrome: a case report
by: Clancy Cerejo, et al.
Published: (2024-11-01) -
Assessment of vascular tortuosity in 22q11.2 deletion syndrome using optical coherence tomography angiography
by: Luca Lucchino, et al.
Published: (2025-06-01) -
Investigational Management for a Positive NIPT Result - Case Report
by: Elena Evelina STOICA, et al.
Published: (2024-06-01)