HYPERTROPHIC CARDIOMYOPATHY IN MUCOPOLYSACCHARIDOSES - REGRESSION AFTER BONE-MARROW TRANSPLANTATION

被引：31

作者：

VINALLONGA, X

SANZ, N

BALAGUER, A

MIRO, L

ORTEGA, JJ

CASALDALIGA, J

机构：

[1] UNIV AUTONOMA BARCELONA,UNIDAD CARDIOL PEDIAT,BARCELONA,SPAIN

[2] UNIV AUTONOMA BARCELONA,UNIDAD HEMATOL PEDIAT,BARCELONA,SPAIN

[3] HOSP INFANTIL VALLE HEBRON,SECC CIRURG CARDIOVASC PEDIAT,BARCELONA,SPAIN

[4] HOSP MATERNO INFANTIL VALLE HEBRON,SERV PEDIAT,BARCELONA,SPAIN

来源：

PEDIATRIC CARDIOLOGY | 1992年 / 13卷 / 02期

关键词：

MUCOPOLYSACCHARIDOSES; HYPERTROPHIC CARDIOMYOPATHY; BONE MARROW TRANSPLANTATION;

D O I：

10.1007/BF00798216

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

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.

引用

页码：107 / 109

页数：3