Congenital pulmonary airway malformation | Zendy

Ghamartaj Khanbabaee | Zendy; S A Tabatabaei | Zendy; F. Rahimpoor | Zendy; Alireza Khatami | Zendy; F. Jadali | Zendy; Javad Ghoroobi | Zendy; Kourosh Sheibani | Zendy; Nima Rezaei | Zendy

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Congenital pulmonary airway malformation

Author(s) -

Ghamartaj Khanbabaee,

S A Tabatabaei,

F. Rahimpoor,

Alireza Khatami,

F. Jadali,

Javad Ghoroobi,

Kourosh Sheibani,

Nima Rezaei

Publication year - 2013

Publication title -

bratislavské lekárske listy/bratislava medical journal

Language(s) - Uncategorized

Resource type - Journals

SCImago Journal Rank - 0.387

H-Index - 32

eISSN - 1336-0345

pISSN - 0006-9248

DOI - 10.4149/bll_2013_126

Subject(s) - medicine , lung , cyst , respiratory system , erythrocyte sedimentation rate , white blood cell , pathology , surgery , gastroenterology

Congenital cystic adenomatoid malformations (CCAMs) are considered rare developmental anomalies of the lower respiratory tract. These are hamartomatous abnormalities of the lung with adenomatoid proliferation of cysts resembling bronchioles and ususally occur sporadically occur and unilaterally with single lobe involvement.

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