Restrictive cardiomyopathy due to storage disease (Q96351): Difference between revisions

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Cardiomiopatia restritiva devido à doença de depósito é a presença de cardiomiopatia restritiva na presença de um glicogênio, esfingolipidoses (como deficiência de α-galactosidase-A (doença de Anderson-Fabry)), mucopolissacaridoses (como deficiência de α-l iduronidase (síndrome de Hurler)), sobrecarga de ferro (como hemocromatose) ou outro transtorno de depósito conhecido por estar significativamente associado à cardiomiopatia restritiva.
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Restrictive cardiomyopathy due to storage disease is the presence of restrictive cardiomyopathy in the presence of a glycogen, sphingolipidoses (such as α-galactosidase-A deficiency (Anderson-Fabry disease)), mucopolysaccharidoses (such as α-l iduronidase deficiency (Hurler syndrome)), iron-overload (such as haemochromatosis), or other storage disorder known to be significantly associated with restrictive cardiomyopathy.

Revision as of 12:19, 16 August 2026

Restrictive cardiomyopathy due to storage disease is the presence of restrictive cardiomyopathy in the presence of a glycogen, sphingolipidoses (such as α-galactosidase-A deficiency (Anderson-Fabry disease)), mucopolysaccharidoses (such as α-l iduronidase deficiency (Hurler syndrome)), iron-overload (such as haemochromatosis), or other storage disorder known to be significantly associated with restrictive cardiomyopathy.
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    English
    Restrictive cardiomyopathy due to storage disease
    Restrictive cardiomyopathy due to storage disease is the presence of restrictive cardiomyopathy in the presence of a glycogen, sphingolipidoses (such as α-galactosidase-A deficiency (Anderson-Fabry disease)), mucopolysaccharidoses (such as α-l iduronidase deficiency (Hurler syndrome)), iron-overload (such as haemochromatosis), or other storage disorder known to be significantly associated with restrictive cardiomyopathy.

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