Clinical Manifestations and Genotype of Primary Ciliary Dyskinesia Diagnosed in Korea: Multicenter Study

PURPOSE: Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder that leads to secondary ciliary dysfunction. PCD is a rare disease, and data on it are limited in Korea. This study systematically evaluated the clinical symptoms, diagnostic characteristics, and treatment modalities o...

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Detalles Bibliográficos
Autores principales: Kim, Minji, Lee, Mi-Hee, Hong, Soo-Jong, Yu, Jinho, Cho, Joongbum, Suh, Dong In, Kim, Hyung Young, Kim, Hye-Young, Jung, Sungsu, Lee, Eun, Lee, Sooyoung, Jeong, Kyunguk, Shim, Jung Yeon, Kim, Jeong Hee, Chung, Hai Lee, Jang, Yoon Young, Kwon, Ji-Won, Seo, Ju-Hee, Kim, Ju Hee, Ahn, Ji Young, Song, Kun-Baek, Song, Kyu-Sang, Kim, So Yeon, Kim, Seon Young, Kil, Hong Ryang, Chung, Eun Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Asthma, Allergy and Clinical Immunology; The Korean Academy of Pediatric Allergy and Respiratory Disease 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643857/
https://www.ncbi.nlm.nih.gov/pubmed/37957793
http://dx.doi.org/10.4168/aair.2023.15.6.757

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10643857/
https://www.ncbi.nlm.nih.gov/pubmed/37957793
http://dx.doi.org/10.4168/aair.2023.15.6.757

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