Lipofuscinose Ceroide Neuronal
Autossómica recessiva
Um grupo de doenças cerebrais degenerativas progressivas hereditárias, caracterizadas clinicamente por um declínio das capacidades mentais e de outras funções, por epilepsia e por perda de visão devido à degeneração da retina, e histopatologicamente pela acumulação intracelular de um material autofluorescente, a lipofuscina ceroide, nas células neuronais do cérebro e da retina.
Também conhecida como
ceroid lipofuscinoses; NCL
Inclui 39 subtipos relacionados ↓Ocultar subtipos ↑
- adult neuronal ceroid lipofuscinosis
- adult neuronal ceroid lipofuscinosis 1
- adult neuronal ceroid lipofuscinosis 5
- ceroid lipofuscinosis, neuronal, 4 (Kufs type)
- ceroid lipofuscinosis, neuronal, 6A
- ceroid lipofuscinosis, neuronal, 6B (Kufs type)
- congenital neuronal ceroid lipofuscinosis
- congenital neuronal ceroid lipofuscinosis 10
- infantile neuronal ceroid lipofuscinosis
- infantile neuronal ceroid lipofuscinosis 1
- infantile neuronal ceroid lipofuscinosis 2
- juvenile neuronal ceroid lipofuscinosis
- juvenile neuronal ceroid lipofuscinosis 1
- juvenile neuronal ceroid lipofuscinosis 10
- juvenile neuronal ceroid lipofuscinosis 2
- juvenile neuronal ceroid lipofuscinosis 3
- juvenile neuronal ceroid lipofuscinosis 5
- juvenile neuronal ceroid lipofuscinosis 6
- late infantile neuronal ceroid lipofuscinosis 1
- late infantile neuronal ceroid lipofuscinosis 10
- late infantile neuronal ceroid lipofuscinosis 2
- late infantile neuronal ceroid lipofuscinosis 5
- late infantile neuronal ceroid lipofuscinosis 6
- late infantile neuronal ceroid lipofuscinosis 8
- neuronal ceroid lipofuscinosis 1
- neuronal ceroid lipofuscinosis 10
- neuronal ceroid lipofuscinosis 11
- neuronal ceroid lipofuscinosis 13
- neuronal ceroid lipofuscinosis 15
- neuronal ceroid lipofuscinosis 2
- neuronal ceroid lipofuscinosis 3
- neuronal ceroid lipofuscinosis 5
- neuronal ceroid lipofuscinosis 7
- neuronal ceroid lipofuscinosis 8
- neuronal ceroid lipofuscinosis 8 northern epilepsy variant
- neuronal ceroid lipofuscinosis 9
- parkinsonism due to ATP13A2 deficiency
- progressive myoclonic epilepsy type 3
- protracted juvenile neuronal ceroid lipofuscinosis 3
