Skip Navigation LinksHome > April 2012 - Volume 12 - Issue 2 > Congenital Disorder of Glycosylation: A Case Presentation
Advances in Neonatal Care:
doi: 10.1097/ANC.0b013e318241bc1b
Case of the Month

Congenital Disorder of Glycosylation: A Case Presentation

Snow, Timothy M. RN, MSN, NNP-BC; Woods, Christopher W. RN, MSN, NNP-BC; Woods, Amanda G. RN, MSN, NNP-BC

Section Editor(s): HEABERLIN, PAMELA

Collapse Box

Abstract

Congenital disorders of glycosylation (CDG) are a group of rare genetically inherited disorders that involve the malfunction of attaching sugar molecules to lipids, proteins, or other organic molecules through an enzymatic process. The resulting defect in glycoprotein and glycolipid synthesis often has a heterogeneous range of multisystemic effects ranging from mild dysmorphism to profound organ failure and subsequent death. There are 2 types of CDG, type I and type II, with multiple subtypes within each. This column is a case presentation about an infant who presented with CDG type Ik.

© 2012 National Association of Neonatal Nurses

Login

Search for Similar Articles
You may search for similar articles that contain these same keywords or you may modify the keyword list to augment your search.