Urban–Rogers–Meyer syndrome

Urban–Rogers–Meyer syndrome
Classification and external resources
Specialty	medical genetics
ICD-10	Q87.8
OMIM	264010

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

↑ Online 'Mendelian Inheritance in Man' (OMIM) 264010
↑ Urban MD, Rogers JG, Meyer WJ (Jan 1979). "Familial syndrome of mental retardation, short stature, contractures of the hands, and genital anomalies". J. Pediatr. 94 (1): 52–55. doi:10.1016/S0022-3476(79)80349-2. PMID 758422.
1 2 Pagnan NA, Gollop TR (Dec 1988). "Prader-Willi habitus, osteopenia, and camptodactyly (Urban–Rogers–Meyer syndrome): a probable second report". Am. J. Med. Genet. 31 (4): 787–792. doi:10.1002/ajmg.1320310410. PMID 3239569.
↑ "Urban Rogers Meyer syndrome". Orphanet. Retrieved Aug 29, 2010.
↑ "Urban-Rogers-Meyer syndrome". Jablonski's Syndromes Database (closed). NLM. Retrieved Aug 29, 2010.

External links

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.

Congenital abnormality syndromes (Q87, 759.7)

Craniofacial

Acrocephalosyndactylia Apert syndrome/Pfeiffer syndrome Saethre–Chotzen syndrome Carpenter syndrome Sakati–Nyhan–Tisdale syndrome

other:	Möbius syndrome Goldenhar syndrome Cyclopia Baller–Gerold syndrome

Short stature

Limbs

Adducted thumb syndrome Holt–Oram syndrome Klippel–Trénaunay–Weber syndrome Nail–patella syndrome Rubinstein–Taybi syndrome

Gastrulation/mesoderm:	Caudal regression syndrome ectromelia Sirenomelia VACTERL association

Overgrowth

Laurence–Moon–Bardet–Biedl

Combined/other,
known locus

2 (Feingold syndrome)
3 (Zimmermann–Laband syndrome)
4/13 (Fraser syndrome)
8 (Branchio-oto-renal syndrome, CHARGE syndrome)
12 (Keutel syndrome, Timothy syndrome)
15 (Marfan syndrome)
19 (Donohue syndrome)
Multiple
- Fryns syndrome

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