Врожденный гипопитуитаризм при делециях 18 хромосомы

Congenital hypopituitarism is a rare disease. It can be caused by isolated inborn defects of the pituitary, gene mutations (PROP1, PIT1), and chromosomal abnormalities.Deletions of chromosome 18 (De Grouchy syndrome types 1 and 2) are a group of rare genetic diseases with a frequency of 1:50,000. Hy...

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Detalles Bibliográficos
Autores principales: Болмасова, А. В., Меликян, М. А., Гаджиева, З. Ш., Пучкова, А. А., Дегтярева, А. В., Петеркова, В. А.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrinology Research Centre 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753836/
https://www.ncbi.nlm.nih.gov/pubmed/34533014
http://dx.doi.org/10.14341/probl12761

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753836/
https://www.ncbi.nlm.nih.gov/pubmed/34533014
http://dx.doi.org/10.14341/probl12761

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