New case of syncytial giant-cell variant of hepatocellular carcinoma in a pediatric patient with HNF1B deficiency: does it fit with the syndrome?
Background Hepatocyte nuclear factor 1B (HNF1B) is a member of the homeodomain-containing family of transcription factors located on 17q12. HNF1B deficiency is associated with a clinical syndrome (kidney and urogenital malformations, maturity-onset diabetes of the young, exocrine pancreatic insuffic...
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| Main Authors: | Michele Pinon, Pier Luigi Calvo, Davide Tinti, Silvia Kalantari, Luca Fabris, Massimiliano Cadamuro, Alessandro Gambella, Renato Romagnoli, Laura Giugliano, Cristina Chiadò, Valeria Bracciamà, Silvia Deaglio, Licia Peruzzi, Roberta Cotti, Silvia Catalano |
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| Format: | Article |
| Language: | English |
| Published: |
BMJ Publishing Group
2022-10-01
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| Series: | BMJ Open Gastroenterology |
| Online Access: | https://bmjopengastro.bmj.com/content/9/1/e001013.full |
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