Quality of life in Italian patients with Multiple endocrine neoplasia type 1 (MEN 1): results of an extensive survey

BACKGROUND: MEN1 is a complex, rare, syndrome inherited in an autosomal dominant tract and characterized by the development of multiple neuroendocrine tumors, requiring lifelong surveillance and multiple medical and surgical therapies throughout the patient’s life. For all these reasons, a diagnosis...

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Bibliografiske detaljer
Udgivet i:Orphanet J Rare Dis
Main Authors: Giusti, Francesca, Cioppi, Federica, Fossi, Caterina, Marini, Francesca, Masi, Laura, Tonelli, Francesco, Brandi, Maria Luisa
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2021
Fag:
Research
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7788910/
https://ncbi.nlm.nih.gov/pubmed/33407684
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-01650-y
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