Nakajo-Nishimura Syndrome: The First African Case
Nakajo-Nishimura Syndrome: The First African Case
About this item
Full title
Author / Creator
Publisher
Athens: PCO Convin S.A
Journal title
Language
English
Formats
Publication information
Publisher
Athens: PCO Convin S.A
Subjects
More information
Scope and Contents
Contents
Nakajo-Nishimura syndrome is a hereditary autoinflammatory disorder caused by an autosomal recessive homozygous mutation of the PSMB8 gene, which encodes the immunoproteasome subunit beta 5i. The clinical manifestations of NNS are mainly pernio-like skin rashes, nodular erythema, lipodystrophy, clubbed fingers, remittent fever, hepatosplenomegaly,...
Alternative Titles
Full title
Nakajo-Nishimura Syndrome: The First African Case
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10466351
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10466351
Other Identifiers
ISSN
2529-198X
E-ISSN
2529-198X
DOI
10.31138/mjr.34.2.262
