Document Detail


Hypertrophic cardiomyopathy in mucopolysaccharidoses: regression after bone marrow transplantation.
MedLine Citation:
PMID:  1614914     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Mucopolysaccharide storage disease (MPS) presents clinically with a broad spectrum of abnormalities, among which cardiovascular involvement has been described. The echocardiographic findings have recently been reported for the various types of MPS. Among these, asymmetric septal hypertrophy (ASH) has been documented. We present a case of a 9-year-old girl suffering from type I MPS, atypical variant, with echocardiographic signs of ASH. She was given a bone marrow transplant after which the hypertrophic cardiomyopathy regressed.
Authors:
X Viñallonga; N Sanz; A Balaguer; L Miro; J J Ortega; J Casaldaliga
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Pediatric cardiology     Volume:  13     ISSN:  0172-0643     ISO Abbreviation:  Pediatr Cardiol     Publication Date:  1992 Apr 
Date Detail:
Created Date:  1992-07-29     Completed Date:  1992-07-29     Revised Date:  2008-02-20    
Medline Journal Info:
Nlm Unique ID:  8003849     Medline TA:  Pediatr Cardiol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  107-9     Citation Subset:  IM    
Affiliation:
Unidad de Cardiología Pediátrica, Universidad Autónoma de Barcelona, Spain.
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MeSH Terms
Descriptor/Qualifier:
Bone Marrow Transplantation*
Cardiomyopathy, Hypertrophic / therapy*,  ultrasonography
Child
Echocardiography
Female
Follow-Up Studies
Humans
Mucopolysaccharidosis I / therapy*,  ultrasonography

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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