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dc.contributor.authorEmre, Senol
dc.contributor.authorSarimurat, Nuevit
dc.date.accessioned2021-03-03T17:04:50Z
dc.date.available2021-03-03T17:04:50Z
dc.identifier.citationSarimurat N., Emre S., "Bronchopulmonary malformations and congenital diaphragmatic hernia", TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, cilt.45, ss.68-71, 2010
dc.identifier.issn1306-0015
dc.identifier.othervv_1032021
dc.identifier.otherav_47da96f7-51a9-47b6-a599-b7d51ff4ad79
dc.identifier.urihttp://hdl.handle.net/20.500.12627/51823
dc.identifier.urihttps://doi.org/10.4274/tpa.45.68
dc.description.abstractAirways with lung parenchyma and foregut develop from primitive foregut. Bronchopulmonary foregut molformations are the name of congenital, structural, often sporadic and non-hereditary anomalies including vessel anomalies formes during individual development of these two system following their separation from each other. The wideley observed forms are summarise in the context of this article. Congenital diaphragmatic hernia (CDH) is a disease that is coused by the incomplete maturation of the diaphragm and a defect mostly on the left side, at the postero-lateral portion of the diaphragm. Diaphragm completes its growth around 4th-8th gestational age. If not then the abdominal viscera moves into the thoracic cavity and lung development is insufficient due to compression of the abdominal organs. This also causes maturation problem at the pulmonary arteries and ends up with severe pulmonary hipertansion that might be highly fatal in the newborns. (Turk Arch Ped 2010; 45 Suppl: 68-71)
dc.language.isoeng
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.titleBronchopulmonary malformations and congenital diaphragmatic hernia
dc.typeMakale
dc.relation.journalTURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume45
dc.identifier.startpage68
dc.identifier.endpage71
dc.contributor.firstauthorID76367


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