Congenital central hypoventilation syndrome, report of three cases
OBJECTIVE: To evaluate clinical characteristics and PHOX2B gene mutations in congenital central hypoventilation syndrome (CCHS) and to facilitate the early diagnosis and management of CCHS and reduce the misdiagnosis
Publié dans: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 51(2013), 11 vom: 31. Nov., Seite 852-5 |
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Auteur principal: | |
Autres auteurs: | , , |
Format: | Article |
Langue: | Chinese |
Publié: |
2013
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Accès à la collection: | Zhonghua er ke za zhi = Chinese journal of pediatrics |
Sujets: | Case Reports English Abstract Journal Article Homeodomain Proteins NBPhox protein Transcription Factors Carbon Dioxide 142M471B3J Alanine OF5P57N2ZX |