Myotonic dystrophy type 1 (Q85709): Difference between revisions
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A doença de Steinert, também conhecida como distrofia miotônica tipo 1, é uma doença do músculo esquelético caracterizada por miotonia e por dano multiorgânico que combina vários graus de fraqueza muscular, arritmia e / ou distúrbios de condução cardíaca, catarata, disfunção endócrina, distúrbios do sono e calvície. | |||
| description / en | description / en | ||
Steinert disease, also known as myotonic dystrophy type 1, is a skeletal muscle disease characterised by myotonia and by multiorgan damage that combines various degrees of muscle weakness, arrhythmia and/or cardiac conduction disorders, cataract, endocrine damage, sleep disorders and baldness. | |||
Revision as of 11:04, 15 August 2026
Steinert disease, also known as myotonic dystrophy type 1, is a skeletal muscle disease characterised by myotonia and by multiorgan damage that combines various degrees of muscle weakness, arrhythmia and/or cardiac conduction disorders, cataract, endocrine damage, sleep disorders and baldness.
| Language | Label | Description | Also known as |
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| default for all languages | ID_557405480 |
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| English | Myotonic dystrophy type 1 |
Steinert disease, also known as myotonic dystrophy type 1, is a skeletal muscle disease characterised by myotonia and by multiorgan damage that combines various degrees of muscle weakness, arrhythmia and/or cardiac conduction disorders, cataract, endocrine damage, sleep disorders and baldness. |
