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Published in 2019 at "Critical Care Medicine"
DOI: 10.1097/01.ccm.0000551930.81980.d9
Abstract: Learning Objectives: Hunter syndrome (MPS II) is a rare genetic disorder with accumulation of glycosaminoglycan resulting in short stature, hepatosplenomegaly, joint stiffness, cardiac valvular disease and airway involvement including macroglossia, tracheal deformities, laryngomalacia, and obstructive…
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Keywords:
patient;
hunter syndrome;
failure patient;
respiratory failure ... See more keywords