Blau syndrome with hypertension and hepatic granulomas: a case report and literature review
BackgroundBlau syndrome (BS) is a monogenic disorder caused by NOD2 gene variants characterized by the triad of granulomatous polyarthritis, rash, and uveitis. Atypical symptoms were recognized in one-third to one-half of individuals with BS. This study aims to describe the clinical features of BS p...
Saved in:
Main Authors: | Fangling Yao (Author), Bei Tan (Author), Di Wu (Author), Min Shen (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2023-07-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Blau syndrome: a case report from Palestine
by: Salam Iriqat, et al.
Published: (2021) -
Blau syndrome: A case report of a rare granulomatous disorder
by: Preema Sinha, et al.
Published: (2020) -
A Chinese girl of Blau syndrome with renal arteritis and a literature review
by: Qiaoqian Zeng, et al.
Published: (2023) -
Identification of Blau Syndrome disease signatures
by: Valencia X, et al.
Published: (2011) -
Blau syndrome complicated by granulomatous tubulointerstitial nephritis and immune complex mediated glomerulonephritis: A case report and review of the literature
by: Kelly M. Garrity, et al.
Published: (2024)