Pitt Hopkins-Like Syndrome 1 with Novel CNTNAP2 Mutation in Siblings.

Mittal, Rea; Kumar, Ashutosh; Ladda, Roger; Mainali, Gayatra; Aliu, Ermal

Mittal, Rea; Kumar, Ashutosh; Ladda, Roger; Mainali, Gayatra; Aliu, Ermal.

Afiliação

Mittal R; Penn State Health College of Medicine, Hershey, USA.
Kumar A; Department of Pediatrics and Neurology, Penn State Health College of Medicine, Hershey, USA.
Ladda R; Department of Pediatrics, Penn State Health College of Medicine, Hershey, USA.
Mainali G; Department of Pediatrics and Neurology, Penn State Health College of Medicine, Hershey, USA.
Aliu E; Department of Pediatrics, Penn State Health College of Medicine, Hershey, USA.

Child Neurol Open ; 8: 2329048X211055330, 2021.

Article em En | MEDLINE | ID: mdl-34778490

Palavras-chave

CNTNAP2; cortical dysplasia-focal epilepsy syndrome; developmental delay; epilepsy; intellectual disability; pediatrics; pitt Hopkins-like syndrome 1

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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