Juvenile neuronal ceroid lipofuscinosis (Q89122): Difference between revisions
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As lipofuscinoses ceróides neuronais juvenis são um grupo geneticamente heterogêneo de lipofuscinoses ceróides neuronais, tipicamente caracterizadas pelo início na idade escolar precoce com perda de visão devido a retinopatia, convulsões e declínio das capacidades mentais e motoras. | |||
| description / en | description / en | ||
Juvenile neuronal ceroid lipofuscinoses are a genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterised by onset at early school age with vision loss due to retinopathy, seizures and the decline of mental and motor capacities. | |||
Revision as of 15:39, 15 August 2026
Juvenile neuronal ceroid lipofuscinoses are a genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterised by onset at early school age with vision loss due to retinopathy, seizures and the decline of mental and motor capacities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1716107919 |
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| English | Juvenile neuronal ceroid lipofuscinosis |
Juvenile neuronal ceroid lipofuscinoses are a genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterised by onset at early school age with vision loss due to retinopathy, seizures and the decline of mental and motor capacities. |
