A New MEN2 Syndrome with Clinical Features of Both MEN2A and MEN2B Associated with a New
Journal
Case reports in endocrinology
ISSN: 2090-6501
Titre abrégé: Case Rep Endocrinol
Pays: United States
ID NLM: 101576457
Informations de publication
Date de publication:
2020
2020
Historique:
received:
14
01
2020
accepted:
25
03
2020
entrez:
18
8
2020
pubmed:
18
8
2020
medline:
18
8
2020
Statut:
epublish
Résumé
Multiple endocrine neoplasia type 2 (MEN2) is a hereditary cancer syndrome caused by This is the first case of a complex syndrome characterized by peculiar features of MEN2B, without Pheo but with a pelvic plexiform neurofibroma and with HPTH, which is typical of MEN2A. A "de novo" new germline
Sections du résumé
BACKGROUND
BACKGROUND
Multiple endocrine neoplasia type 2 (MEN2) is a hereditary cancer syndrome caused by
CONCLUSIONS
CONCLUSIONS
This is the first case of a complex syndrome characterized by peculiar features of MEN2B, without Pheo but with a pelvic plexiform neurofibroma and with HPTH, which is typical of MEN2A. A "de novo" new germline
Identifiants
pubmed: 32802527
doi: 10.1155/2020/4147097
pmc: PMC7411486
doi:
Types de publication
Case Reports
Langues
eng
Pagination
4147097Informations de copyright
Copyright © 2020 Carlotta Giani et al.
Déclaration de conflit d'intérêts
The authors declare that there are no conflicts of interest regarding the publication of this article.
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