paraplejía espástica, atrofia óptica y neuropatía y trastorno relacionado con paraplejía espástica, atrofia óptica y neuropatía
A group of rare genetic neurodegenerative diseases with characteristics of infancy to childhood onset of progressive spastic paraplegia (with delayed motor milestones, gait disturbances, hyperreflexia and extensor plantar responses), optic atrophy (w
SNOMEDCT-ES (trastorno) / 789674008
SNOMEDCT-ES (with delayed motor milestones, gait disturbances, hyperreflexia and extensor plantar responses), optic atrophy (w / 789674008