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Up to: Spondyloepimetaphyseal dysplasia · TRPV4-related bone disorder
Spondyloepimetaphyseal dysplasia, Maroteaux type
A very rare type of spondyloepiphyseal dysplasia described in fewer than 10 patients to date and characterized clinically by dysplastic epiphyses, short stature appearing in infancy, short neck, short and stubby hands and feet, scoliosis, genu valgum, abnormal pelvis, osteoporosis and osteoarthritis.
This condition has no sub-types.