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Treatment response to Janus kinase inhibitor in a child affected by Aicardi-Goutières syndrome.
Galli, Jessica; Cattalini, Marco; Loi, Erika; Ferraro, Rosalba Monica; Giliani, Silvia; Orcesi, Simona; Pinelli, Lorenzo; Badolato, Raffaele; Fazzi, Elisa.
Afiliação
  • Galli J; Department of Clinical and Experimental Sciences University of Brescia Brescia Italy.
  • Cattalini M; Unit of Child Neurology and Psychiatry ASST Spedali Civili of Brescia Brescia Italy.
  • Loi E; Department of Clinical and Experimental Sciences University of Brescia Brescia Italy.
  • Ferraro RM; Pediatrics Clinic ASST Spedali Civili of Brescia Brescia Italy.
  • Giliani S; Department of Clinical and Experimental Sciences University of Brescia Brescia Italy.
  • Orcesi S; Department of Molecular and Translational Medicine University of Brescia Brescia Italy.
  • Pinelli L; "Angelo Nocivelli" Institute for Molecular Medicine, ASST Spedali Civili of Brescia Brescia Italy.
  • Badolato R; Department of Molecular and Translational Medicine University of Brescia Brescia Italy.
  • Fazzi E; "Angelo Nocivelli" Institute for Molecular Medicine, ASST Spedali Civili of Brescia Brescia Italy.
Clin Case Rep ; 11(8): e7724, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37534202
Key Clinical Message: Baricitinib, a Janus kinase inhibitor (JAK-inhibitor), seems to contribute to an improvement of a child affected by Aicardi-Goutières syndrome (AGS), reducing the interferon score and determining a recovery of cognitive, communicative, and relational dysfunctions, while the gross motor deficit persisted. Abstract: We report the treatment response to baricitinib, a JAK-inhibitor, in a 4-year-old girl affected by Aicardi-Goutières syndrome (AGS2, RNASEH2B mutation). Using quantitative measures, we detected a significant amelioration characterized by a complete recovery of cognitive, communicative, and relational skills after 8 and 16 months from the beginning of therapy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2023 Tipo de documento: Article