Wilms tumour resulting from paternal transmission of a TRIM28 pathogenic variant-A first report.
James WhitworthRuth ArmstrongEamonn R MaherPublished in: European journal of human genetics : EJHG (2024)
Wilms tumour (nephroblastoma) is a renal embryonal tumour that is frequently caused by constitutional variants in a small range of cancer predisposition genes. TRIM28 has recently been identified as one such gene. Previously, observational data strongly suggested a parent of origin effect, whereby Wilms tumour only occurred following maternal inheritance of a pathogenic genetic variant. However, here we report a child with bilateral Wilms tumour who had inherited a pathogenic TRIM28 variant from their father. This finding suggests that genetic counselling for paternally inherited pathogenic variants in TRIM28 should include discussion of a potential risk of Wilms tumour.
Keyphrases
- copy number
- genome wide
- mitochondrial dna
- mental health
- electronic health record
- cross sectional
- squamous cell carcinoma
- pregnant women
- body mass index
- papillary thyroid
- climate change
- genome wide identification
- smoking cessation
- case report
- human immunodeficiency virus
- hiv infected
- artificial intelligence
- deep learning
- bioinformatics analysis