Ehlers-Danlos/osteogenesis imperfecta syndrome is an association of the features of Ehlers-Danlos syndrome and osteogenesis imperfecta, characterized by generalized joint hypermobility and dislocations, skin hyperextensibility and/or translucency, and easy bruising as the predominant clinical features, while being invariably associated with mild signs of osteogenesis imperfecta, including short stature, blue sclera, and osteopenia or fractures.
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Ehlers-Danlos syndrome, classic type
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Ehlers-Danlos syndrome, hypermobility type
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Ehlers-Danlos syndrome, arthrochalasia type
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Ehlers-Danlos syndrome, spondylodysplastic type
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Ehlers-Danlos syndrome, periodontitis type
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Ehlers-Danlos syndrome, autosomal dominant, type unspecified
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