Congenital neuronal ceroid lipofuscinosis (Q89120): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Verification Status | |||
Concluído | |||
| Property / Verification Status: Concluído / rank | |||
Normal rank | |||
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 |
|---|---|---|---|
| default for all languages | ID_641209188 |
||
| 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. |
Statements
CID11:ID_641209188
0 references
dki-india-ID_641209188
0 references
Concluído
0 references
