Hereditary osteo-onycho-renal dysplasia with excess urinary pyridinoline cross-links and abnormal kidney collagen cross-linking

B Lubec, K Arbeiter, W Ulrich, G Frauscher - Nephron, 1995 - karger.com
B Lubec, K Arbeiter, W Ulrich, G Frauscher
Nephron, 1995karger.com
HOOD syndrome is a rare genetic disorder also known as nail patella syndrome.
Biochemical and molecular biological data are rare and not conclusive. Preliminary data
suggest the involvement of collagen type IV. This would, however, not be enough to explain
nail or bone involvement. As kidney pathology would be consistent with a cross-linking
disorder, we tested collagen IV and kidney collagen cross-linking on SDS-PAGE. This
method showed a remarkable reduction in high-molecular-weight collagen polymers. The …
Abstract
HOOD syndrome is a rare genetic disorder also known as nail patella syndrome. Biochemical and molecular biological data are rare and not conclusive. Preliminary data suggest the involvement of collagen type IV. This would, however, not be enough to explain nail or bone involvement. As kidney pathology would be consistent with a cross-linking disorder, we tested collagen IV and kidney collagen cross-linking on SDS-PAGE. This method showed a remarkable reduction in high-molecular-weight collagen polymers. The patient’s and his mother’s urinary pyridinoline cross-link excretion was manifold increased. Disturbed cross-linking of connective tissue proteins would help to explain the multiorgan involvement.
Karger