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BAP1 Tumour Predisposition Syndrome Due to Whole BAP1 Gene Deletion.

Dinusha PandithanSonja KlebeGrace McKavanaghLesley RawlingsSui YuJillian NichollNicola K Poplawski
Published in: Case reports in genetics (2022)
BRCA-1-associated protein-1 (BAP1) tumour predisposition syndrome (BAP1-TPDS) is a dominant hereditary cancer syndrome. The full spectrum of associated malignancies is yet to be fully characterised. We detail the phenotypic features of the first reported family with a whole BAP1 gene deletion. This report also adds to the emerging evidence that the rhabdoid subtype of meningioma is a part of the clinical spectrum of this tumour predisposition syndrome.
Keyphrases
  • case report
  • genome wide
  • squamous cell carcinoma
  • dna methylation
  • transcription factor
  • squamous cell
  • genome wide analysis