Title of article
Congenital diaphragmatic hernia: searching for answers
Author/Authors
John R. Gosche، نويسنده , , Saleem Islam، نويسنده , , Scott C. Boulanger، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2005
Pages
9
From page
324
To page
332
Abstract
Background
Pulmonary hypoplasia and hypertension are the primary causes of morbidity and mortality in infants with congenital diaphragmatic hernia (CDH). At present, the origin of CDH and the causes of pulmonary hypoplasia and hypertension are unknown.
Data Sources
This article reviews the available published data regarding the origin of CDH and the pathogenesis of the associated pulmonary hypertension and hypoplasia. These investigations have employed human tissues as well as two types of CDH animal models.
Conclusions
Investigations performed to date have not yet provided definitive answers regarding the pathogenesis of CDH. However, they have yielded many new and exciting discoveries and several opportunities for intervention. Ongoing research should open new possibilities to improve the outcome for these unfortunate babies with CDH.
Keywords
Pulmonary hypoplasia , Branching morphogenesis , congenital diaphragmatic hernia , pulmonary hypertension
Journal title
The American Journal of Surgery
Serial Year
2005
Journal title
The American Journal of Surgery
Record number
618020
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