AP incidence
Musculoskeletal system
Case TypeClinical Cases
AuthorsMoreira, Adriana; Portugal, Inês; Carneiro, Alexandre; Castro, Miguel
Patient17 years, female
[1] Daston MM, Scrable H, Nordlund M, Sturbaum AK, Nissen LM, Ratner N. (1992) The protein product of the neuro bromatosis type 1 gene is expressed at highest abundance in neurons, Schwann cells, and oligodendrocytes. Neuron 8:415–428 (PMID: 1550670)
[2] Kolanczyk M, Kossler N, Kuhnisch J, et al. (2007) Multiple roles for neurofibromin in skeletal development and growth. Human Molecular Genetics 16:874– 886 (PMID: 17317783)
[3] Patel NB, Stacy GS (2012) Musculoskeletal manifestations of neurofibromatosis type 1. American Journal of Roentgenology 199(1):W99-106. (PMID: 22733937)
[4] Crawford AH, Schorry EK (2006) Neurofibromatosis update. Journal of Pediatric Orthopaedics 26:413–423 (PMID: 16670560)
[5] Howlett DC, Farrugia MM, Ferner RE, Rankin SC. (1998) Multiple lower limb non-ossifying bromas in siblings with neuro bromatosis. European Journal of Radiology 26:280–283 (PMID: 9587756)
[6] Charles YP, Diméglio A, Chammas M. (2009) Congenital pseudarthrosis of the forearm. Report of two cases and review of the literature. Chirurgie de la Main Feb;28(1):26-32 (PMID: 19097927)
[7] Ramelli GP, Slongo T, Tschäppeler H, Weis J (2001) Congenital pseudarthrosis of the ulna and radius in two cases of neurofibromatosis type 1. Pediatric surgery international 17(2-3) : 239-41 (PMID: 11315302)
URL: | https://eurorad.org/case/14069 |
DOI: | 10.1594/EURORAD/CASE.14069 |
ISSN: | 1563-4086 |
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.