Se la conosci la riconosci
La sindrome CHARGE
S. Tajθ, P. Cianci, A. Selicorni
Novembre 2017 - pagg. 585 -586
Suggerite dall'AI
Classificazione MeSH
Contenuto riservato
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Bibliografia
Bergman JE, Janssen N, Hoefsloot LH, Jongmans MC, Hofstra
RM, van Ravenswaaij-Arts CM. CHD7 mutations and CHARGE syndrome:
the clinical implications of an expanding phenotype. J Med
Genet 2011;48(5):334-42.
Blake KD, Davenport SLH, Hall BD, et al. CHARGE association: an
update and review for the primary pediatrician. Clin Pediatr 1998;
37:159-73.
Dobbelsteyn C, Peacocke SD, Blake K, et al. Feeding difficulties in
children with CHARGE syndrome: prevalence, risk factors, and prognosis.
Dysphagia 2008;23(2):127-35.
Hsu P, Ma A, Wilson M, Williams G, et al. CHARGE syndrome: a
review. J Paediatr Child Health 2014;50(7):504-11.
Issekutz KA, Graham JM, Prasad C, et al. An epidemiological
analysis of CHARGE syndrome: preliminary results from a Canadian
study. Am J Med Genet A 2005;133A(3):309-17.
Lalani SR, Hefner MA, Belmont JW, Davenport SLH. CHARGE syndrome.
GeneReviews 2012.
Santoro L, Ficcadenti A, Zallocco F, et al. Cognitive-motor profile,
clinical characteristics and diagnosis of CHARGE syndrome: an Italian
experience. Am J Med Genet A 2014;164A:3042-51.
Verloes A. Update diagnostic criteria for CHARGE syndrome: a
proposal. Am J Med Genet A 2005;133:306-8.
Wineland A, Menezes MD, Shimony JS, Shinawi MS, Hullar TE,
Hirose K. Prevalence of semicircular canal hypoplasia in patients
with CHARGE syndrome: 3C syndrome. JAMA Otolaryngol Head
Neck Surg 2017;143(2):168-77.
Corrispondenza: angelo.selicorni61@gmail.com
