Urban-Rogers-Meyer syndrome

This syndrome is characterized by intellectual deficit, short stature, obesity, genital abnormalities, and hand and/or toe contractures. It has been described in two brothers and in one isolated case. The patients also present with generalized osteoporosis and a history of frequent fractures. This syndrome is similar to Prader-Willi syndrome, but the hand contractures and osteoporosis, together with the lack of hypotonia, indicate this is a different entity.

Also known as: Prader-Willi habitus-osteopenia-camptodactyly syndrome, intellectual disability-short stature-hand contractures-genital anomalies syndrome, urban-Rogers-Meyer syndrome, Prader-Willi habitus, osteopenia, and camptodactyly

0 clinical trials for this condition and its sub-types, 0 tagged with Urban-Rogers-Meyer syndrome itself.