Cargando…

Tofacitinib effectiveness in Blau syndrome: a case series of Chinese paediatric patients

OBJECTIVE: Blau syndrome (BS), a rare, autosomal-dominant autoinflammatory syndrome, is characterized by a clinical triad of granulomatous recurrent uveitis, dermatitis, and symmetric arthritis and associated with mutations of the nucleotide-binding oligomerization domain containing 2 (NOD2) gene. A...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhang, Song, Cai, Zhe, Mo, Xiaolan, Zeng, Huasong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2021
Materias:	Short Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8594202/ https://www.ncbi.nlm.nih.gov/pubmed/34781959 http://dx.doi.org/10.1186/s12969-021-00634-x

Ejemplares similares

Clinical and immunological study of Tofacitinib and Baricitinib in refractory Blau syndrome: case report and literature review
por: Álvarez-Reguera, Carmen, et al.
Publicado: (2022)

A Case of Blau Syndrome
por: Chauhan, Krati, et al.
Publicado: (2014)

Tofacitinib, a suppressor of NOD2 expression, is a potential treatment for Blau syndrome
por: Ueki, Yoko, et al.
Publicado: (2023)

Successful Treatment of Paediatric Morphea with Tofacitinib
por: TANG, Jun-Chi, et al.
Publicado: (2023)

Blau syndrome with persistent fetal vasculature: a case report
por: Liu, Miao, et al.
Publicado: (2023)

Sinus of valsalva aneurysm in Blau's syndrome
por: Mourad, Faisal, et al.
Publicado: (2010)

A New Mutation in Blau Syndrome
por: Zeybek, Cengiz, et al.
Publicado: (2015)

Blau syndrome: a case report from Palestine
por: Iriqat, Salam, et al.
Publicado: (2021)

Effective treatment of TNFα inhibitors in Chinese patients with Blau syndrome
por: Chen, Jing, et al.
Publicado: (2019)

Etanercept-Induced Myelopathy in a Pediatric Case of Blau Syndrome
por: Caracseghi, Fabiola, et al.
Publicado: (2011)

A Case of Sporadic Blau Syndrome with an Uncommon Clinical Course
por: Imayoshi, Miyoko, et al.
Publicado: (2018)

65. Blau syndrome treated with sequential biologics
por: Yi Yong, Cee, et al.
Publicado: (2018)

72. A retrospective diagnosis of Blau syndrome
por: Ellis, Jessica, et al.
Publicado: (2018)

A Chinese girl of Blau syndrome with renal arteritis and a literature review
por: Zeng, Qiaoqian, et al.
Publicado: (2023)

Tofacitinib for the treatment of lichen planopilaris: A case series
por: Yang, Christine C., et al.
Publicado: (2018)

Identification of Blau Syndrome disease signatures
por: Foley, KP, et al.
Publicado: (2011)

NOD2 mosaicism in Blau syndrome
por: Mensa-Vilaro, A, et al.
Publicado: (2015)

A new mutation in blau syndrome: case report
por: Zeybek, Cengiz, et al.
Publicado: (2014)

NOD2 Mutation-Associated Case with Blau Syndrome Triggered by BCG Vaccination
por: Arakawa, Akiko, et al.
Publicado: (2021)

Characterization of Blau syndrome panuveitis with wide-field fluorescein angiography
por: DeSouza, Philip J., et al.
Publicado: (2019)

Aortoarteritis and cardiomyopathy in a child with Blau Syndrome
por: Khubchandani, RP, et al.
Publicado: (2011)

Blau syndrome: An under-reported condition in India?
por: Agarwal, A, et al.
Publicado: (2022)

Diagnostics challenges and therapeutic response in Blau syndrome – case report
por: Paim-Marque, Luciana B, et al.
Publicado: (2014)

Familial Blau syndrome: First molecularly confirmed report from India
por: Janarthanan, Mahesh, et al.
Publicado: (2019)

Manifestation of Panuveitis after Intraocular Surgery in a Child with Blau Syndrome
por: Magliyah, Moustafa S., et al.
Publicado: (2021)

Clinical phenotype and CARD15 gene mutation with Blau Syndrome in Chinese children and their parents
por: Li, C, et al.
Publicado: (2008)

A familial case of Blau syndrome caused by a novel NOD2 genetic mutation
por: Kim, Woojoong, et al.
Publicado: (2016)

Blau Syndrome, the prototypic auto-inflammatory granulomatous disease
por: Wouters, Carine H, et al.
Publicado: (2014)

EP25 Blau syndrome: a lifetime of sarcoid
por: Chauhan, Neal, et al.
Publicado: (2020)

NOD2/CARD15 gene mutation identified in a Chinese family with Blau syndrome
por: Xiang, Haotian, et al.
Publicado: (2012)

Ophthalmological treatment of early-onset sarcoidosis/Blau syndrome in a Colombian child: A case report
por: Marín-Noriega, María Alejandra, et al.
Publicado: (2020)

A novel mutation in early‐onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes
por: Okazaki, Fumiko, et al.
Publicado: (2021)

Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome
por: Chang, Shao-Yu, et al.
Publicado: (2022)

A diagnostic challenge: misdiagnosing Blau syndrome as juvenile dermatomyositis in a pediatric patient
por: Deek, Soud M.S., et al.
Publicado: (2023)

Blau syndrome with hypertension and hepatic granulomas: a case report and literature review
por: Yao, Fangling, et al.
Publicado: (2023)

Detection of Mycobacterium avium ss. Paratuberculosis in Blau Syndrome Tissues
por: Dow, C. Thomas, et al.
Publicado: (2010)

OR3-002 – Blau Syndrome cohort study: ocular outcome
por: Rose, CD, et al.
Publicado: (2013)

Tofacitinib in Hypertrophic Lichen Planus
por: SEIRINGER, Peter, et al.
Publicado: (2020)

Uveitis in sporadic Blau syndrome: Long-term follow-up of a refractory case treated successfully with adalimumab
por: Naik, Anmol U, et al.
Publicado: (2018)

Tofacitinib in Refractory Scleritis: A Case Series
por: Dey, Suvankar, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_q6k2ksp3n5iffc0qgc5nrenhfj