International Scholarly Research Notices / 2012 / Article / Fig 2

Review Article

Ehlers-Danlos Syndrome, Hypermobility Type: An Underdiagnosed Hereditary Connective Tissue Disorder with Mucocutaneous, Articular, and Systemic Manifestations

Figure 2

Skin and mucosal features of Ehlers-Danlos syndrome, hypermobility type. Atrophic, nonpapyraceous scar—its atrophic nature is more appreciable after gentle squeezing between examinator’s fingers (a). Accentuated crease reticulum of the palm (b). Keratosis pilaris in a 26-year-old woman (c). Piezogenic papules at wrists after compression (d). Extensive abdominal striae atrophicae in a 35-year-old multipara (e). Postsurgical scar with anetoderma-like herniation of the subcutaneous fat (f). Apparent absence of the lingual frenulum (g). Radiographic orthopanoramic showing extensive tooth loss in a 50-year-old man with severe gingival involvement (h). Blue sclerae (i).
751768.fig.002a
(a)
751768.fig.002b
(b)
751768.fig.002c
(c)
751768.fig.002d
(d)
751768.fig.002e
(e)
751768.fig.002f
(f)
751768.fig.002g
(g)
751768.fig.002h
(h)
751768.fig.002i
(i)

Article of the Year Award: Outstanding research contributions of 2020, as selected by our Chief Editors. Read the winning articles.