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
Suggerite dall'AI
Classificazione MeSH
Contenuto riservato
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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
