Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups.

Assmann, Gunter; Köhm, Michaela; Schuster, Volker; Behrens, Frank; Mössner, Rotraut; Magnolo, Nina; Oji, Vinzenz; Burkhardt, Harald; Hüffmeier, Ulrike

Assmann, Gunter; Köhm, Michaela; Schuster, Volker; Behrens, Frank; Mössner, Rotraut; Magnolo, Nina; Oji, Vinzenz; Burkhardt, Harald; Hüffmeier, Ulrike.

Afiliação

Assmann G; Department of Internal Medicine I, José-Carreras Centrum for Immuno- and Gene Therapy, University of Saarland Medical School, /Saar, Homburg, Germany.
Köhm M; Division of Rheumatology and IME, Fraunhofer Institute, Branch for Translational Medicine and Pharmacology, Goethe University, Frankfurt am Main, Germany.
Schuster V; Hospital for Children and Adolescents, University of Leipzig, Leipzig, Germany.
Behrens F; Division of Rheumatology and IME, Fraunhofer Institute, Branch for Translational Medicine and Pharmacology, Goethe University, Frankfurt am Main, Germany.
Mössner R; Department of Dermatology, Georg-August-University Göttingen, Göttingen, Germany.
Magnolo N; Department of Dermatology, University of Münster, Münster, Germany.
Oji V; Department of Dermatology, University of Münster, Münster, Germany.
Burkhardt H; Division of Rheumatology and IME, Fraunhofer Institute, Branch for Translational Medicine and Pharmacology, Goethe University, Frankfurt am Main, Germany.
Hüffmeier U; Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Schwabachanlage 10, 91054, Erlangen, Germany. ulrike.hueffmeier@uk-erlangen.de.

BMC Med Genet ; 21(1): 102, 2020 05 12.

Article em En | MEDLINE | ID: mdl-32397996

Assuntos

Síndrome de Hiperostose Adquirida/genética; Moléculas de Adesão Celular/genética; Proteínas do Citoesqueleto/genética; Predisposição Genética para Doença; Osteomielite/genética; Síndrome de Hiperostose Adquirida/fisiopatologia; Adolescente; Adulto; Criança; Feminino; Humanos; Hiperostose/genética; Hiperostose/fisiopatologia; Masculino; Osteomielite/fisiopatologia; Psoríase/genética; Psoríase/fisiopatologia; Fatores de Risco

Palavras-chave

Association; Chronic non-bacterial osteomyelitis (CNO); Chronic recurrent multifocal osteomyelitis (CRMO); Coding variants; Syndrome of synovitis acne pustulosis hyperostosis osteitis (SAPHO (syndrome))

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteomielite / Moléculas de Adesão Celular / Síndrome de Hiperostose Adquirida / Predisposição Genética para Doença / Proteínas do Citoesqueleto Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: BMC Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha

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