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The Ehlers‐Danlos syndrome: an analysis of the structure of the collagen fibres of the skin
Author(s) -
BLACK CAROL M.,
GATHERCOLE L. J.,
BAILEY A. J.,
BEIGHTON P.
Publication year - 1980
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/j.1365-2133.1980.tb05675.x
Subject(s) - ultrastructure , transmission electron microscopy , collagen fibres , collagen fibril , electron microscope , fibril , ehlers–danlos syndrome , anatomy , pathology , chemistry , medicine , materials science , dermatology , biology , biophysics , optics , nanotechnology , physics
SUMMARY The structure of the collagen fibres of the skin in the Ehlers‐Danlos syndrome (ED‐S) was studied in eight patients with ED‐S Type I., three patients with ED‐S Type II and three patients with the X‐linked Type V. The results show that the reducible cross‐links are present and undergo the same maturation process to non‐reducible cross‐links as in normal skin. Transmission electron microscopy revealed a normal ultrastructure of the collagen fibrils. At a higher morphological level of organization scanning electron microscopy demonstrated progressive increase in fibre bundle disorder from the X‐linked to mitis, to gravis, in which the fibres making up the large fibre bundles demonstrated a considerable inability to aggregate.