Congenital neuronal ceroid lipofuscinosis (Q89120): Difference between revisions
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A lipofuscinose ceróide neuronal congênita é uma forma grave de lipofuscinose ceróide neuronal com início ao nascimento, caracterizada por microcefalia primária, epilepsia neonatal e morte na primeira infância. | |||
| description / en | description / en | ||
Congenital neuronal ceroid lipofuscinosis (CNCL) is a severe form of neuronal ceroid lipofuscinosis (NCL) with onset at birth characterised by primary microcephaly, neonatal epilepsy, and death in early infancy. | |||
Revision as of 15:39, 15 August 2026
Congenital neuronal ceroid lipofuscinosis (CNCL) is a severe form of neuronal ceroid lipofuscinosis (NCL) with onset at birth characterised by primary microcephaly, neonatal epilepsy, and death in early infancy.
| Language | Label | Description | Also known as |
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| default for all languages | ID_641209188 |
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| English | Congenital neuronal ceroid lipofuscinosis |
Congenital neuronal ceroid lipofuscinosis (CNCL) is a severe form of neuronal ceroid lipofuscinosis (NCL) with onset at birth characterised by primary microcephaly, neonatal epilepsy, and death in early infancy. |
