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

Abstract 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 a...

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Main Authors: Roberta Onesimo (Author), Rita De Santis (Author), Chiara Leoni (Author), Mario Rigante (Author), Marco Piastra (Author), Elisabetta Sforza (Author), Angelo Selicorni (Author), Giuseppe Zampino (Author)
Format: Book
Published: BMC, 2023-07-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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