Literature DB >> 27537080

Musculoskeletal and overgrowth syndromes associated with cutaneous abnormalities.

Bahar Dasgeb1, Michael A Morris2, Christina M Ring1, Darius Mehregan3, Michael E Mulligan2.   

Abstract

There are cutaneous abnormalities that are characteristic to certain peculiar musculoskeletal conditions. The understanding of associated imaging and clinical skin findings together in this context can play an important role for the dermatologist and radiologist in establishing the correct diagnoses. The scope of dermatological manifestations of many acquired diseases of the soft tissues, muscles or bone is broad. Therefore, the intent of this article is to review those entities that are genetic and/or inherited. The goal of this review is to develop a better understanding of the cases presented. In these cases, collaboration between dermatologists and radiologists may be paramount to generating a diagnosis and monitoring at-risk patients.

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Mesh:

Year:  2016        PMID: 27537080      PMCID: PMC5124849          DOI: 10.1259/bjr.20160521

Source DB:  PubMed          Journal:  Br J Radiol        ISSN: 0007-1285            Impact factor:   3.039


  39 in total

1.  Imaging findings of fibrous dysplasia with histopathologic and intraoperative correlation.

Authors:  Kimberly A Fitzpatrick; Mihra S Taljanovic; Donald P Speer; Anna R Graham; Jon A Jacobson; George R Barnes; Tim B Hunter
Journal:  AJR Am J Roentgenol       Date:  2004-06       Impact factor: 3.959

2.  Imaging characteristics of tuberous sclerosis.

Authors:  D G Bell; B F King; R R Hattery; J W Charboneau; A D Hoffman; O W Houser
Journal:  AJR Am J Roentgenol       Date:  1991-05       Impact factor: 3.959

Review 3.  Focal dermal hypoplasia: oral and dental findings.

Authors:  Zahra Tejani; Puneet Batra; Carol Mason; David Atherton
Journal:  J Clin Pediatr Dent       Date:  2005       Impact factor: 1.065

4.  Failure of rapamycin in the treatment of multiple haemangiomas associated with Maffucci syndrome.

Authors:  Z Li; B Zhao; Y Zhang; C Tu; Y Zheng; X He; S Xiao
Journal:  Clin Exp Dermatol       Date:  2015-01-27       Impact factor: 3.470

5.  Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis.

Authors:  Miriam J Smith; Andrew J Wallace; Naomi L Bowers; Cecilie F Rustad; C Geoff Woods; Guy D Leschziner; Rosalie E Ferner; D Gareth R Evans
Journal:  Neurogenetics       Date:  2012-03-22       Impact factor: 2.660

6.  Buschke-Ollendorff syndrome.

Authors:  Donatella Schena; Lerica Germi; Maria Rosa Zamperetti; Chiara Colato; Giampiero Girolomoni
Journal:  Int J Dermatol       Date:  2008-11       Impact factor: 2.736

Review 7.  Marfan syndrome-diagnosis and management.

Authors:  Naser M Ammash; Thoralf M Sundt; Heidi M Connolly
Journal:  Curr Probl Cardiol       Date:  2008-01       Impact factor: 5.200

Review 8.  Gorlin-Goltz syndrome in a child: case report and clinical review.

Authors:  A Snoeckx; F M Vanhoenacker; K Verhaert; K Chappelle; P M Parizel
Journal:  JBR-BTR       Date:  2008 Nov-Dec

9.  Enchondroma versus chondrosarcoma in the appendicular skeleton: differentiating features.

Authors:  M D Murphey; D J Flemming; S R Boyea; J A Bojescul; D E Sweet; H T Temple
Journal:  Radiographics       Date:  1998 Sep-Oct       Impact factor: 5.333

10.  Mortality associated with neurofibromatosis 1: a cohort study of 1895 patients in 1980-2006 in France.

Authors:  Tu Anh Duong; Emilie Sbidian; Laurence Valeyrie-Allanore; Cédric Vialette; Salah Ferkal; Smaïl Hadj-Rabia; Christophe Glorion; Stanislas Lyonnet; Michel Zerah; Isabelle Kemlin; Diana Rodriguez; Sylvie Bastuji-Garin; Pierre Wolkenstein
Journal:  Orphanet J Rare Dis       Date:  2011-05-04       Impact factor: 4.123

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  1 in total

Review 1.  Imaging More than Skin-Deep: Radiologic and Dermatologic Presentations of Systemic Disorders.

Authors:  Mehrzad Shafiei; Firoozeh Shomal Zadeh; Bahar Mansoori; Hunter Pyle; Nnenna Agim; Jorge Hinojosa; Arturo Dominguez; Cristina Thomas; Majid Chalian
Journal:  Diagnostics (Basel)       Date:  2022-08-19
  1 in total

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