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Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants

Detalles Bibliográficos
Autores principales: Trupiano, Nicole, Koeppe, Erika, Jacobs, Michelle F., Else, Tobias, Cha, Kelly B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731975/
https://www.ncbi.nlm.nih.gov/pubmed/36505034
http://dx.doi.org/10.1016/j.jdcr.2022.10.034
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author Trupiano, Nicole
Koeppe, Erika
Jacobs, Michelle F.
Else, Tobias
Cha, Kelly B.
author_facet Trupiano, Nicole
Koeppe, Erika
Jacobs, Michelle F.
Else, Tobias
Cha, Kelly B.
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spelling pubmed-97319752022-12-10 Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants Trupiano, Nicole Koeppe, Erika Jacobs, Michelle F. Else, Tobias Cha, Kelly B. JAAD Case Rep Case Report Elsevier 2022-11-07 /pmc/articles/PMC9731975/ /pubmed/36505034 http://dx.doi.org/10.1016/j.jdcr.2022.10.034 Text en © 2022 Published by Elsevier on behalf of the American Academy of Dermatology, Inc. This is an open access.. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Trupiano, Nicole
Koeppe, Erika
Jacobs, Michelle F.
Else, Tobias
Cha, Kelly B.
Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants
title Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants
title_full Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants
title_fullStr Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants
title_full_unstemmed Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants
title_short Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants
title_sort rare presentations can suggest more than one rare condition: striking personal and family cancer history in a patient with both cdkn2a and brca1 pathogenic variants
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731975/
https://www.ncbi.nlm.nih.gov/pubmed/36505034
http://dx.doi.org/10.1016/j.jdcr.2022.10.034
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