Prader-Willi Habitus, Osteopenia, And Camptodactyly

Prader-Willi habitus, osteopenia, and camptodactyly syndrome is characterized by intellectual disability, short stature, obesity, genital abnormalities, and hand and/or toe contractures. It has only been described in two brothers and in one isolated case in a different family. Other symptoms included unusual face, deformity of the spinal column, osteoporosis and a history of frequent fractures. It is similar to syndrome/resources/1" target="_blank">Prader-Willi syndrome, but the authors concluded that it is a different condition. The cause was unknown in the reported cases.