ACUTE INFANTILE CARDIOMYOPATHY AS A PRESENTING FEATURE OF MUCOPOLYSACCHARIDOSIS-VI

被引：30

作者：

HAYFLICK, S

ROWE, S

KAVANAUGHMCHUGH, A

OLSON, JL

VALLE, D

机构：

[1] JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, PCTB 802, 725 N WOLFE ST, BALTIMORE, MD 21205 USA

[2] JOHNS HOPKINS UNIV, SCH MED, CTR MED GENET, BALTIMORE, MD 21205 USA

[3] JOHNS HOPKINS UNIV, SCH MED, DIV PEDIAT CARDIOL, BALTIMORE, MD 21205 USA

[4] JOHNS HOPKINS UNIV, SCH MED, DEPT PATHOL, BALTIMORE, MD 21205 USA

[5] JOHNS HOPKINS UNIV, SCH MED, HOWARD HUGHES MED INST, GENET LAB, BALTIMORE, MD 21205 USA

来源：

JOURNAL OF PEDIATRICS | 1992年 / 120卷 / 02期

关键词：

D O I：

10.1016/S0022-3476(05)80441-X

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

An infant with a diagnosis of acute infantile cardiomyopathy was subsequently shown to have mucopolysaccharidosis VI. The mucopolysaccharidoses should be included in the differential diagnosis of infantile cardiomyopathy.

引用

页码：269 / 272

页数：4

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