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|Title:||Usefulness of bone marrow transplantation in the Hurler syndrome|
|Citation:||American Journal of Cardiology, 2003; 92(7):882-886|
|Publisher:||Excerpta Medica Inc|
|Elizabeth A. Braunlin, Nanci R. Stauffer, Charles H. Peters, John L. Bass, James M. Berry, John J. Hopwood and William Krivit|
|Abstract:||The Hurler syndrome, an autosomal recessive storage disease of childhood, leads to death within the first decade of life from progressive deposition of glycosaminoglycans within the myointima of the coronary arteries and airways. Cardiac ultrasound findings of patients with this syndrome >10 years after successful bone marrow transplantation are described.|
|Keywords:||Humans; Heart Diseases; Mucopolysaccharidosis I; Ultrasonography; Bone Marrow Transplantation; Follow-Up Studies; Time; Adolescent; Child; Outcome Assessment (Health Care); Female; Male; Cardiovascular Physiological Phenomena|
|Rights:||Copyright © 2003 Excerpta Medica Inc. All rights reserved.|
|Appears in Collections:||Paediatrics publications|
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