Urinary pyridinoline cross-links as biomarkers of osteogenesis imperfecta.
Data(s) |
2015
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Resumo |
Osteogenesis imperfecta (OI) is a group of genetic heterogeneous connective tissue disorders characterized by increased bone fragility and susceptibility to fractures. Laboratory diagnosis relies on time-consuming and cost-intensive biochemical and molecular genetics analyses. Therefore, it is desirable to identify and establish new diagnostic markers for OI that are reliable, cost-effective and easily accessible. In our study we have identified the ratio of the urinary pyridinoline cross-links lysyl-pyridinoline and hydroxylysyl-pyridinoline as a promising, time- and cost-effective biomarker for osteogenesis imperfecta, that could be used furthermore to investigate cases of suspected non-accidental injury in infants. |
Identificador |
https://serval.unil.ch/?id=serval:BIB_3C9B6096429E isbn:1750-1172 (Electronic) pmid:26306627 doi:10.1186/s13023-015-0315-9 isiid:000360039000001 |
Idioma(s) |
en |
Fonte |
Orphanet Journal of Rare Diseases, vol. 10, no. 1, pp. 104 |
Palavras-Chave | #Amino Acids/urine; Biomarkers/urine; Humans; Mutation; Osteogenesis Imperfecta/genetics; Osteogenesis Imperfecta/urine |
Tipo |
info:eu-repo/semantics/article article |