Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
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Pediatria flash

Iperlassità legamentosa e bambini

Valentina Carrato, Giovanna Ferrara

Scuola di Specializzazione in Pediatria, Università di Trieste

Marzo 2017 - pagg. 182 -184

a cura di Irene Bruno
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Bibliografia
• Castori M, Dordoni C, Valiante M, et al. Nosology and inheritance pattern(s) of joint hypermobility syndrome and Ehlers-Danlos syndrome, hypermobility type: a study of intrafamilial and interfamilial variability in 23 Italian pedigrees. Am J Med Genet A 2014;164A: 3010-20. • Cattalini M, Khubchandani R, Cimaz R. When flexibility is not necessarily a virtue: a review of hypermobility syndromes and chronic or recurrent musculoskeletal pain in children. Pediatr Rheumatol Online J 2015;13:40. • Grahame R, Bird HA, Child A. The revised (Brighton 1998) criteria for the diagnosis of benign joint hypermobility syndrome (BJHS). J Rheumatol 2000;27:1777. • Groth KA, Stochholm K, Hove H, et al. Aortic events in a nationwide Marfan syndrome cohort. Clin Res Cardiol 2017;106(2):105-12. • Hakim A, Grahame R. Joint hypermobility. Best Pract Res Clin Rheumatol 2003;17:989-1004. • Loeys BL, Dietz HC, Braverman AC, et al. The revised Ghent nosology for the Marfan syndrome. J Med Genet 2010;47:476-85. • MacCarrick G, Black JH 3rd, Bowdin S, et al. Loeys-Dietz syndrome: a primer for diagnosis and management. Genet Med 2014;16:576-87. • Mathias CJ, Low DA, Iodice V, et al. Postural tachycardia syndrome - current experience and concepts. Nat Rev Neurol 2011;8:22. • Rezvani I, Rosenblatt DS. Homocystinuria. In: Kliegman R, Stanton B, St Geme J, Schor N. Nelson Textbook of Pediatrics, 20th edition. Elsevier Health Sciences (Eds) 2016;644-6. • Stickler syndrome. Genereviews 2014. • Tinkle BT, Bird HA, Grahame R, et al. The lack of clinical distinction between the hypermobility type of Ehlers-Danlos syndrome and the joint hypermobility syndrome (a.k.a. hypermobility syndrome). Am J Med Genet A 2009;149A:2368. • Verstraeten A, Alaerts M, Van Laer L, et al. Marfan Syndrome and related disorders: 25 years of gene discovery. Hum Mutat 2016;37: 524-31.

Corrispondenza: irene.bruno@burlo.trieste.it