Coinheritance of naevoid basal cell carcinoma syndrome and neurofibromatosis type 1 associated with an exceptional spectrum of tumours.

Ghadiri, S J; Brennan, P; Calonje, E; Carmichael, A J; Rajan, N

Ghadiri, S J; Brennan, P; Calonje, E; Carmichael, A J; Rajan, N.

Afiliação

Ghadiri SJ; Department of Dermatology, James Cook University Hospital, Middlesbrough, TS4 3BW, UK.
Brennan P; Clinical Genetics, James Cook University Hospital, Middlesbrough, TS4 3BW, UK.
Calonje E; Department of Dermatopathology, St John's Institute of Dermatology, St Thomas' Hospital, London, SE1 7EH, UK.
Carmichael AJ; Department of Dermatology, James Cook University Hospital, Middlesbrough, TS4 3BW, UK.
Rajan N; Department of Dermatology, Royal Victoria Infirmary, Newcastle upon Tyne, NE1 4LP, UK.

Br J Dermatol ; 183(6): 1108-1110, 2020 12.

Article em En | MEDLINE | ID: mdl-32562549

Assuntos

Síndrome do Nevo Basocelular; Carcinoma Basocelular; Neurofibromatose 1; Neoplasias Cutâneas; Síndrome do Nevo Basocelular/genética; Humanos; Neurofibromatose 1/complicações; Neoplasias Cutâneas/genética

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Carcinoma Basocelular / Síndrome do Nevo Basocelular / Neurofibromatose 1 Idioma: En Ano de publicação: 2020 Tipo de documento: Article

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