Fetuin-A deficiency is associated with infantile cortical hyperostosis (Caffey disease)
Sign Up to like & getrecommendations! Published in 2019 at "Pediatric Research"
DOI: 10.1038/s41390-019-0499-0
Abstract: BackgroundInfantile cortical hyperostosis (ICH)/Caffey disease is an inflammatory collagenopathy of infancy, manifested by subperiosteal bone hyperplasia. Genetically, ICH was linked with heterozygosity for an R836C mutation in the COL1A1 gene. Although an autosomal-recessive trait is… read more here.
Keywords: cortical hyperostosis; fetuin deficiency; deficiency; caffey disease ... See more keywords
Fetuin-A Deficiency but Not Pentraxin 3, FGF-21, or Irisin, Predisposes to More Serious COVID-19 Course
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DOI: 10.3390/biom11101422
Abstract: Analysis of liver biopsy specimens showed that SARS-CoV-2 might have led to liver damage. This study aimed to evaluate the role of selected hepatokines and myokines in the development and progression of COVID-19. Seventy patients… read more here.
Keywords: covid patients; fgf; fetuin deficiency; covid course ... See more keywords