Chinese case of Nakajo-Nishimura syndrome with a novel mutation of the PSMB8 gene

J Dermatol. 2019 May;46(5):e160-e161. doi: 10.1111/1346-8138.14679. Epub 2018 Nov 2.

Authors

Xiuyan Shi^{1

2}, Xin Xiang¹, Zhaoyang Wang¹, Lin Ma¹, Zigang Xu¹

Affiliations

¹ Department of Dermatology, Beijing Children's Hospital, Capital Medical University, Beijing, China.
² Department of Dermatology, Liaocheng People's Hospital and Clinical School of Taishan Medical University, Liaocheng, China.

PMID: 30387862
DOI: 10.1111/1346-8138.14679

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Asian People / genetics
Child, Preschool
DNA Mutational Analysis
Erythema Nodosum / diagnosis
Erythema Nodosum / genetics*
Erythema Nodosum / pathology
Fingers / abnormalities*
Fingers / pathology
Genetic Testing
Humans
Male
Mutation
Proteasome Endopeptidase Complex / genetics*
Skin / pathology

Substances

LMP7 protein
Proteasome Endopeptidase Complex

Supplementary concepts

Nakajo syndrome