Peroxisomal acyl-CoA oxidase deficiency (Q88705): Difference between revisions
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A deficiência de acil-CoA oxidase peroxissomal é uma doença neurodegenerativa rara que pertence ao grupo das doenças peroxissomais hereditárias e é caracterizada por hipotonia e convulsões no período neonatal e regressão neurológica na primeira infância. | |||
| description / en | description / en | ||
Peroxisomal acyl-CoA oxidase deficiency is a rare neurodegenerative disorder that belongs to the group of inherited peroxisomal disorders and is characterised by hypotonia and seizures in the neonatal period and neurological regression in early infancy. | |||
Revision as of 15:05, 15 August 2026
Peroxisomal acyl-CoA oxidase deficiency is a rare neurodegenerative disorder that belongs to the group of inherited peroxisomal disorders and is characterised by hypotonia and seizures in the neonatal period and neurological regression in early infancy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_927825451 |
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| English | Peroxisomal acyl-CoA oxidase deficiency |
Peroxisomal acyl-CoA oxidase deficiency is a rare neurodegenerative disorder that belongs to the group of inherited peroxisomal disorders and is characterised by hypotonia and seizures in the neonatal period and neurological regression in early infancy. |
