Resumo

ROBLES-BERMEJO, Fernando; FOURNIER-DEL CASTILLO, María Concepción; GUTIERREZ-SOLANA, Luis González  e  LOPEZ-MARIN, Laura. Neuropsychological profile of a patient with late infantile Krabbe disease and visual agnosia. Rev. mex. pediatr. [online]. 2021, vol.88, n.6, pp.244-248.  Epub 15-Ago-2022. ISSN 0035-0052.  https://doi.org/10.35366/105427.

Krabbe disease is a type of autosomal recessive lysosomal leukodystrophy caused by deficiency of the enzyme galactosylceramidase. The results of the neuropsychological evaluation in a three-year-old boy with apperceptive visual agnosia and prosopagnosia are presented.

Palavras-chave : Apperceptive agnosia; cognitive decline; Krabbe’s disease; neuropsychological assessment; prosopagnosia.

        · resumo em Espanhol     · texto em Espanhol     · Espanhol ( pdf )