Spheroid body myopathy (Q90771): Difference between revisions
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Revision as of 17:45, 15 August 2026
Spheroid body myopathy is a rare illness classified in the group of the congenital myopathies as a desmin-related neuromuscular disorder, presenting dominant autosomical origin with the beginning of the symptoms in the adult phase. Muscle biopsy discloses characteristic spheroid cytoplasmic bodies.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_83824621 |
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| English | Spheroid body myopathy |
Spheroid body myopathy is a rare illness classified in the group of the congenital myopathies as a desmin-related neuromuscular disorder, presenting dominant autosomical origin with the beginning of the symptoms in the adult phase. Muscle biopsy discloses characteristic spheroid cytoplasmic bodies. |
Statements
CID11:ID_83824621
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