| Urban–Rogers–Meyer syndrome | |
|---|---|
| Other names | Prader–Willi habitus, osteopenia, and camptodactyly |
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| This condition is inherited in an autosomal recessive manner | |
| Specialty |
Medical genetics 
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Urban–Rogers–Meyer syndrome, also known as Prader–Willi habitus, osteopenia, and camptodactyly or Urban syndrome, is an extremely rare inherited congenital disorder first described by Urban et al. (1979). It is characterized by genital anomalies, mental retardation, obesity, contractures of fingers, and osteoporosis, though further complications are known.
Further reading
- Prader–Willi habitus, osteopenia, and camptodactyly; Urban–Rogers–Meyer syndrome at NIH's Office of Rare Diseases
- Jablonski's Syndromes Database: Bibliography
- Camera G, Marugo M, Cohen MM (Nov 1993). "Another postnatal-onset obesity syndrome". Am. J. Med. Genet. 47 (6): 820–822. doi:10.1002/ajmg.1320470605. PMID 8279478.