Nasal polyposis in pediatric patients with Cornelia de Lange syndrome: endoscopic diagnosis, treatment and follow up in two case reports

BACKGROUND: Cornelia de Lange syndrome is a rare genetic disease with otolaryngological involvement. The classic phenotype is characterized by distinctive facial features, intellectual disability, growth delay, hirsutism, and upper-limb reduction. Nasal polyposis was previously reported in associati...

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Detalles Bibliográficos
Autores principales: Onesimo, Roberta, Santis, Rita De, Leoni, Chiara, Rigante, Mario, Piastra, Marco, Sforza, Elisabetta, Selicorni, Angelo, Zampino, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350250/
https://www.ncbi.nlm.nih.gov/pubmed/37455311
http://dx.doi.org/10.1186/s13052-023-01454-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350250/
https://www.ncbi.nlm.nih.gov/pubmed/37455311
http://dx.doi.org/10.1186/s13052-023-01454-3

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