Тяжелые костные осложнения первичного гиперпаратиреоза у молодого пациента с верифицированной мутацией в гене <i>MEN1</i>

Multiple endocrine neoplasia type 1 syndrome (MEN1) is a rare inherited disorder that can include combinations of more than 20 endocrine and non-endocrine tumors. Unfortunately, none of the described MEN1 mutations has been associated with a peculiar clinical phenotype, even within members of the sa...

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Detalles Bibliográficos
Autores principales: Еремкина, А. К., Сазонова, Д. В., Бибик, Е. Е., Шейхова, А. З., Хайриева, А. В., Буклемишев, Ю. В., Мокрышева, Н. Г.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrinology Research Centre 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761876/
https://www.ncbi.nlm.nih.gov/pubmed/35262299
http://dx.doi.org/10.14341/probl12864

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761876/
https://www.ncbi.nlm.nih.gov/pubmed/35262299
http://dx.doi.org/10.14341/probl12864

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