Urban–Rogers–Meyer syndrome

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, mental retardation, obesity, contractures of fingers, and osteoporosis,^[3] though further complications are known.^[4]^[5]

References[edit | edit source]

↑ Online Mendelian Inheritance in Man (OMIM) 264010
↑
↑ ^3.0 ^3.1
↑ "Urban Rogers Meyer syndrome". Orphanet. Retrieved Aug 29, 2010.
↑ "Urban-Rogers-Meyer syndrome". Jablonski's Syndromes Database (closed). NLM. Retrieved Aug 29, 2010.

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v t e Congenital abnormality syndromes
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