Developmental trajectory of MLD (metachromatic leukodystrophy).

Metachromatic Leukodystrophy (MLD): Developmental Trajectories Metachromatic leukodystrophy is an autosomal recessive inherited lysosomal storage disease characterized by deficiency of the enzyme arylsulfatase A (ARSA), causing the accumulation of sulfatides and progressive demyelination of the central and peripheral nervous system. Clinical Forms and Late Childhood Trajectory (typical): It manifests between the first…

CLN development trajectories.

Neuronal Ceroid Lipofuscinosis (CLN): Developmental Trajectories Ceroid neuronal lipofuscinosis (CLN), commonly called Batten disease, group together a set of rare lysosomal-based neurodegenerative disorders characterized by the intralysosomal accumulation of fluorescent ceroid lipofuscin material. Common Path of Symptoms Progressive and rapid loss of visual acuity leading to blindness (to...

Network of associations of Camp de Morvedre.

Associative Network in the Camp de Morvedre Region The Camp de Morvedre region has a collaborative structure of associations aimed at inclusion, family support and therapeutic intervention for minors with functional diversity and neurodevelopmental needs. This network facilitates access to local therapeutic clinics, adapted recreational resources and channels of...