Periodontal Ehlers-Danlos syndrome is associated with leukoencephalopathy.

Kapferer-Seebacher, Ines; Waisfisz, Quinten; Boesch, Sylvia; Bronk, Marieke; van Tintelen, Peter; Gizewski, Elke R; Groebner, Rebekka; Zschocke, Johannes; van der Knaap, Marjo S

Kapferer-Seebacher, Ines; Waisfisz, Quinten; Boesch, Sylvia; Bronk, Marieke; van Tintelen, Peter; Gizewski, Elke R; Groebner, Rebekka; Zschocke, Johannes; van der Knaap, Marjo S.

Afiliação

Kapferer-Seebacher I; Department of Operative and Restorative Dentistry, Medical University of Innsbruck, Anichstr. 35, 6020, Innsbruck, Austria.
Waisfisz Q; Department of Clinical Genetics, VU University Medical Center, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
Boesch S; Department of Neurology, Medical University of Innsbruck, Anichstr. 35, 6020, Innsbruck, Austria.
Bronk M; Department of Clinical Genetics, Academic Medical Center, de Boelelaan 1118, 1081 HV, Amsterdam, The Netherlands.
van Tintelen P; Department of Clinical Genetics, VU University Medical Center, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
Gizewski ER; Department of Clinical Genetics, Academic Medical Center, de Boelelaan 1118, 1081 HV, Amsterdam, The Netherlands.
Groebner R; Department of Neuroradiology, Medical University Innsbruck, Anichstr. 35, 6020, Innsbruck, Austria.
Zschocke J; Division of Human Genetics, Medical University of Innsbruck, Peter-Mayr Str. 1, 6020, Innsbruck, Austria.
van der Knaap MS; Division of Human Genetics, Medical University of Innsbruck, Peter-Mayr Str. 1, 6020, Innsbruck, Austria. johannes.zschocke@i-med.ac.at.

Neurogenetics ; 20(1): 1-8, 2019 03.

Article em En | MEDLINE | ID: mdl-30535813

Assuntos

Encéfalo/patologia; Complemento C1r/genética; Síndrome de Ehlers-Danlos/genética; Leucoencefalopatias/genética; Adulto; Idoso; Ataxia Cerebelar/complicações; Ataxia Cerebelar/diagnóstico; Ataxia Cerebelar/genética; Criança; Síndrome de Ehlers-Danlos/complicações; Síndrome de Ehlers-Danlos/diagnóstico; Feminino; Humanos; Leucoencefalopatias/complicações; Leucoencefalopatias/diagnóstico; Imageamento por Ressonância Magnética/métodos; Masculino; Pessoa de Meia-Idade; Mutação/genética; Linhagem

Palavras-chave

Complement 1; EhlersDanlos; Leukoencephalopathy; Periodontitis; Small vessel disease

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Complemento C1r / Síndrome de Ehlers-Danlos / Leucoencefalopatias Idioma: En Ano de publicação: 2019 Tipo de documento: Article

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