Fanconi-like anemia related to a FANCM mutation

Fanconi anemia is primarily inherited as an autosomal recessive genetic disorder with common delays in diagnosis and challenging treatments. Fanconi anemia patients have a high risk of developing solid tumors, particularly in the head and neck or anogenital regions. The diagnosis of Fanconi anemia i...

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Veröffentlicht in:	European journal of medical genetics 2022-01, Vol.65 (1), p.104399-104399, Article 104399
Hauptverfasser:	Encarnación, J.A., Cerezuela, P., Español, I., García, M.R., Manso, C., De la Fuente, I., Garrigós, N., Viney, A., Minguillon, J., Surrallés, J.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Antineoplastic Agents - adverse effects c1511_1515delGAGTA Carcinoma, Squamous Cell - drug therapy Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - radiotherapy Cisplatin - adverse effects DNA Helicases - genetics FANCM gene Fanconi anemia Fanconi Anemia - genetics Fatal Outcome Humans Male Mutation Targeted therapy Tonsil cancer Tonsillar Neoplasms - drug therapy Tonsillar Neoplasms - genetics Tonsillar Neoplasms - radiotherapy
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