MedStar Authors catalog › Details for: Pulmonary interstitial glycogenosis in a patient with trisomy 21.
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Pulmonary interstitial glycogenosis in a patient with trisomy 21.

by Patel, Manisha.
Citation: Journal of Neonatal-Perinatal Medicine. 9(2):227-31, 2016 May 17.Journal: Journal of neonatal-perinatal medicine.Published: 2016ISSN: 1878-4429.Full author list: Morrison AK; Patel M; Johnson SL; LeGallo R; Teague WG; Vergales B.UI/PMID: 27197936.Subject(s): *Down Syndrome/co [Complications] | Down Syndrome/pp [Physiopathology] | Echocardiography | Fatal Outcome | Female | *Glycogen Storage Disease/pa [Pathology] | *Heart Defects, Congenital/pa [Pathology] | Humans | *Hypertension, Pulmonary/pa [Pathology] | Infant, Newborn | Infant, Premature | *Lung Diseases, Interstitial/pa [Pathology]Institution(s): MedStar Franklin Square Medical CenterDepartment(s): NeonatologyActivity type: Journal Article.Medline article type(s): Case Reports | Journal ArticleDigital Object Identifier: https://dx.doi.org/10.3233/NPM-16915112 (Click here) Abbreviated citation: J Neonatal Perinatal Med. 9(2):227-31, 2016 May 17.Abstract: 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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