Urban–Rogers–Meyer syndrome
Medical condition
From Wikipedia, the free encyclopedia
Urban–Rogers–Meyer syndrome, also known as Prader–Willi habitus, osteopenia, and camptodactyly or Urban syndrome,[1] is an extremely rare inherited congenital disorder first described by Urban et al. (1979).[2][3] It is characterized by genital anomalies, intellectual disability, obesity, contractures of fingers, and osteoporosis,[3] though further complications are known.[4][5]
Other namesPrader–Willi habitus, osteopenia, and camptodactyly
| Urban–Rogers–Meyer syndrome | |
|---|---|
| Other names | Prader–Willi habitus, osteopenia, and camptodactyly |
| |
| This condition is inherited in an autosomal recessive manner | |
| Specialty | Medical genetics  |
