Epidermoid cyst in a patient with Alagille syndrome: Coincidence or connection?

BACKGROUND: Alagille syndrome is a rare genetic syndrome, which arises due to defects in the Notch signaling pathway, resulting in liver, cardiopulmonary, renal, skeletal, and ophthalmologic problems, among others. Epidermoid cysts are rare congenital benign lesions that develop from ectopic ectoder...

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Detalles Bibliográficos
Autores principales: Surapaneni, Akhil, Kuo, John, Wang, Min, Ashour, Ramsey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749940/
https://www.ncbi.nlm.nih.gov/pubmed/33365194
http://dx.doi.org/10.25259/SNI_611_2020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749940/
https://www.ncbi.nlm.nih.gov/pubmed/33365194
http://dx.doi.org/10.25259/SNI_611_2020

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