Hypertrophic cardiomyopathy in mucopolysaccharidoses: Regression after bone marrow transplantation

Xavier Viñallonga; Nuria Sanz; Alberto Balaguer; Luis Miro; Juan J. Ortega; Jaume Casaldaliga

doi:10.1007/BF00798216

Hypertrophic cardiomyopathy in mucopolysaccharidoses: Regression after bone marrow transplantation

Xavier Viñallonga, Nuria Sanz, Alberto Balaguer, Luis Miro, Juan J. Ortega, Jaume Casaldaliga

Department of Paediatrics, Obstetrics and Gynaecology and Preventive Medicine and Public Health

Research output: Contribution to journal › Article › Research › peer-review

31 Citations (Scopus)

Abstract

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. © 1992 Springer-Verlag New York Inc.

Original language	English
Pages (from-to)	107-109
Journal	Pediatric Cardiology
Volume	13
Issue number	2
DOIs	https://doi.org/10.1007/BF00798216
Publication status	Published - 1 Apr 1992

Keywords

Bone marrow transplantation
Hypertrophic cardiomyopathy
Mucopolysaccharidoses

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title = "Hypertrophic cardiomyopathy in mucopolysaccharidoses: Regression after bone marrow transplantation",

abstract = "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. {\textcopyright} 1992 Springer-Verlag New York Inc.",

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AU - Viñallonga, Xavier

AU - Sanz, Nuria

AU - Balaguer, Alberto

AU - Miro, Luis

AU - Ortega, Juan J.

AU - Casaldaliga, Jaume

PY - 1992/4/1

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N2 - 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. © 1992 Springer-Verlag New York Inc.

AB - 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. © 1992 Springer-Verlag New York Inc.

KW - Bone marrow transplantation

KW - Hypertrophic cardiomyopathy

KW - Mucopolysaccharidoses

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