Mucolipidosis type 4 (Q58520): Difference between revisions
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A mucolipidose tipo IV é uma doença de depósito lisossomal caracterizada clinicamente por atraso psicomotor e anormalidades visuais, incluindo opacificação da córnea, degeneração retinal ou estrabismo. | |||
| description / en | description / en | ||
Mucolipidosis type IV (ML IV) is a lysosomal storage disease characterised clinically by psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration, or strabismus. | |||
Revision as of 06:05, 14 August 2026
Mucolipidosis type IV (ML IV) is a lysosomal storage disease characterised clinically by psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration, or strabismus.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_597963317 |
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| English | Mucolipidosis type 4 |
Mucolipidosis type IV (ML IV) is a lysosomal storage disease characterised clinically by psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration, or strabismus. |
