Two different genetic diseases in the same patient: Coincident, concomitant, or causally related?

Graf, Julia; Hellenbroich, Yorck; Veelken, Norbert; Figueroa, Karla P; Wolff, Simone; Pulst, Stefan; Brüggemann, Norbert

Graf, Julia; Hellenbroich, Yorck; Veelken, Norbert; Figueroa, Karla P; Wolff, Simone; Pulst, Stefan; Brüggemann, Norbert.

Afiliação

Graf J; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Hellenbroich Y; Department of Neurology, University of Lübeck, Lübeck, Germany.
Veelken N; Institute of Human Genetics, University of Lübeck, Lübeck, Germany.
Figueroa KP; Department of Pediatrics, Asklepios Klinik Nord-Heidberg, Hamburg, Germany.
Wolff S; Department of Neurology, University of Utah, Salt Lake City, Utah, USA.
Pulst S; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
Brüggemann N; Department of Neurology, University of Utah, Salt Lake City, Utah, USA.

Mov Disord ; 31(4): 491-2, 2016 Apr.

Article em En | MEDLINE | ID: mdl-26900085

Assuntos

Doença de Charcot-Marie-Tooth/genética; Ataxia de Friedreich/genética; Distrofia Miotônica/genética; Adolescente; Humanos; Masculino; Pessoa de Meia-Idade; Linhagem

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia de Friedreich / Doença de Charcot-Marie-Tooth / Distrofia Miotônica Limite: Adolescent / Humans / Male / Middle aged Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Alemanha

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