A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture?

Milone, Roberta; Masson, Riccardo; Di Cosmo, Caterina; Tonacchera, Massimo; Bertini, Veronica; Guzzetta, Andrea; Battini, Roberta

Milone, Roberta; Masson, Riccardo; Di Cosmo, Caterina; Tonacchera, Massimo; Bertini, Veronica; Guzzetta, Andrea; Battini, Roberta.

Afiliação

Milone R; Department of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa, Italy.
Masson R; Developmental Neurology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Di Cosmo C; Department of Endocrinology, AOUP, Pisa, Italy.
Tonacchera M; Department of Endocrinology, AOUP, Pisa, Italy.
Bertini V; Section of Cytogenetics, Medicine of Laboratory Department, AOUP, Pisa, Italy.
Guzzetta A; Department of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa, Italy.
Battini R; Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.

Child Neurol Open ; 6: 2329048X19828881, 2019.

Article em En | MEDLINE | ID: mdl-30793011

Palavras-chave

ataxia; autism spectrum disorder; hypotonia; intellectual disability; motor delay

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Child Neurol Open Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Itália País de publicação: Estados Unidos

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