Pulmonary interstitial glycogenosis in a patient with trisomy 21.
Citation: Journal of Neonatal-Perinatal Medicine. 9(2):227-31, 2016 May 17PMID: 27197936Institution: MedStar Franklin Square Medical CenterDepartment: NeonatologyForm of publication: Journal ArticleMedline article type(s): Case Reports | Journal ArticleSubject headings: *Down Syndrome/co [Complications] | *Glycogen Storage Disease/pa [Pathology] | *Heart Defects, Congenital/pa [Pathology] | *Hypertension, Pulmonary/pa [Pathology] | *Lung Diseases, Interstitial/pa [Pathology] | Down Syndrome/pp [Physiopathology] | Echocardiography | Fatal Outcome | Female | Humans | Infant, Newborn | Infant, PrematureYear: 2016ISSN:- 1878-4429
Item type | Current library | Collection | Call number | Status | Date due | Barcode |
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Journal Article | MedStar Authors Catalog | Article | 27197936 | Available | 27197936 |
Pulmonary interstitial glycogenosis is an interstitial lung disease of childhood that has been increasingly reported over the past decade. Here, we present a case of pulmonary interstitial glycogenosis associated with trisomy 21, pulmonary arterial hypertension, and congenital heart disease in a 34 week premature infant.
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