Late infantile neuronal ceroid lipofuscinosis (Q89128): Difference between revisions
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As lipofuscinoses ceróides neuronais infantis tardias são um grupo geneticamente heterogêneo de lipofuscinoses ceróides neuronais tipicamente caracterizadas por início durante a primeira infância com declínio das capacidades mentais e motoras, epilepsia e perda de visão por degeneração retinal. | |||
| description / en | description / en | ||
Late infantile neuronal ceroid lipofuscinoses are a genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterised by onset during infancy or early childhood with decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration. | |||
Revision as of 15:40, 15 August 2026
Late infantile neuronal ceroid lipofuscinoses are a genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterised by onset during infancy or early childhood with decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1923920542 |
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| English | Late infantile neuronal ceroid lipofuscinosis |
Late infantile neuronal ceroid lipofuscinoses are a genetically heterogeneous group of neuronal ceroid lipofuscinoses (NCLs) typically characterised by onset during infancy or early childhood with decline of mental and motor capacities, epilepsy, and vision loss through retinal degeneration. |
