Tourette syndrome, obsessive compulsive behavior, and dysmorphic features in a patient with deletions at chromosome 18q22.1 and chromosome 13q12.3-q13.1.

Bhatti, D; Balasetti, V; Malgireddy, K; Rush, E T; Torres-Russotto, D

Bhatti, D; Balasetti, V; Malgireddy, K; Rush, E T; Torres-Russotto, D.

Afiliação

Bhatti D; Department of Neurological Sciences, University of Nebraska Medical Center, USA.
Balasetti V; Department of Neurological Sciences, University of Nebraska Medical Center, USA.
Malgireddy K; Department of Neurological Sciences, University of Nebraska Medical Center, USA.
Rush ET; Department of Pediatrics, University of Nebraska Medical Center, USA; Department of Internal Medicine, University of Nebraska Medical Center, USA; Department of Orthopedic Surgery, University of Nebraska Medical Center, USA; Munroe Meyer Institute for Genetics and Rehabilitation, University of Nebra
Torres-Russotto D; Department of Neurological Sciences, University of Nebraska Medical Center, USA. Electronic address: drtorres@unmc.edu.

Parkinsonism Relat Disord ; 32: 133-134, 2016 11.

Article em En | MEDLINE | ID: mdl-27637283

Assuntos

Transtornos Cromossômicos/genética; Anormalidades Craniofaciais/genética; Transtorno Obsessivo-Compulsivo/genética; Síndrome de Tourette/genética; Adulto; Deleção Cromossômica; Cromossomos Humanos Par 13/genética; Cromossomos Humanos Par 18/genética; Humanos; Masculino; Adulto Jovem

Palavras-chave

13q13 deletion; 18q22 deletion; Genetics; Tic disorder; Tics; Tourette syndrome

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Tourette / Anormalidades Craniofaciais / Transtornos Cromossômicos / Transtorno Obsessivo-Compulsivo Idioma: En Ano de publicação: 2016 Tipo de documento: Article

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