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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Scientific Scholar
2020
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| 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 |