Natural history of cognitive development in neuronopathic mucopolysaccharidosis type II (Hunter syndrome): Contribution of genotype to cognitive developmental course.

Seo, Joo-Hyun; Okuyama, Torayuki; Shapiro, Elsa; Fukuhara, Yasuyuki; Kosuga, Motomichi

Seo, Joo-Hyun; Okuyama, Torayuki; Shapiro, Elsa; Fukuhara, Yasuyuki; Kosuga, Motomichi.

Afiliação

Seo JH; Clinical Laboratory Medicine, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-8535, Japan.
Okuyama T; Clinical Laboratory Medicine, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-8535, Japan.
Shapiro E; Center for Lysosomal Storage Diseases, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-8535, Japan.
Fukuhara Y; Department of Pediatrics, University of Minnesota Twin Cities, Minneapolis, MN 55455, United States of America.
Kosuga M; Division of Medical Genetics, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-8535, Japan.

Mol Genet Metab Rep ; 24: 100630, 2020 Sep.

Article em En | MEDLINE | ID: mdl-32775211

Palavras-chave

AEq, age equivalent scores; BSID-III, Bayley Scale of Infant Development- Third Edition; CA, chronological age; Cognitive natural history; Developmental age; Genotype; Hunter syndrome; KSPD, Kyoto Scale of Psychological Development; Kyoto Scale of Psychological Development; Mucopolysaccharidosis type II

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Mol Genet Metab Rep Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão

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