A young female of Cowden syndrome presenting with Lhermitte-Duclos disease: An illustrative case

BACKGROUND: Lhermitte-Duclos Disease (LDD), or dysplastic gangliocytoma, which is a benign hamartomatous condition involving the cerebellum, has a possible association with Cowden syndrome (CS), a rare autosomal dominant disorder due to germline mutations in the phosphatase and tensin homolog (PTEN)...

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Detalles Bibliográficos
Autores principales: Al-Noman, Abdullah, Mokbul, Mobin Ibne, Hossain, Nadia, Rana, Md. Sumon, Hasan, Md. Motasimul, Islam, Md. Shafiqul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481842/
https://www.ncbi.nlm.nih.gov/pubmed/37680909
http://dx.doi.org/10.25259/SNI_325_2023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481842/
https://www.ncbi.nlm.nih.gov/pubmed/37680909
http://dx.doi.org/10.25259/SNI_325_2023

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