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Coffee, B., Keith, K., Albizua, I., Malone, T., Mowrey, J., Sherman, S.L. and Warren, S.T. (2009) Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. American Journal of Human Genetics, 85(4), 503-514.

has been cited by the following article:

• TITLE: Dental treatment of twin monozygotic brothers with Fragile X syndrome

  AUTHORS: Flavia Melo Meira, Luis Candido Pinto Silva, Regina Haddad Rezek Ferreira, Roberval Almeida Cruz

  KEYWORDS: Syndromes Head and Neck/cleft Lip and Palate; Fragile X Syndrome; Pain Control/Sedation; Oral Medicine

  JOURNAL NAME: Health, Vol.2 No.10, October 26, 2010

  ABSTRACT: Fragile X syndrome (FXS) is the main cause of inherited mental retardation and is the result of transcriptional silencing of the fragile X mental retardation gene FMR1. An absence of the associated protein FMRP leads to the deregulation of many genes, which results in phenotypes of Attention-Deficit Hyperactivity Disorder (ADHD), anxiety, epilepsy and autism. The aim of this article is to report the clinical case of twin siblings affected by FXS and to describe the procedures for dental treatment with intravenous sedation. Information regarding the characteristic manifestations of FXS not only aided in the handling of the patients but also enabled us to develop clinical programs to promote and maintain oral health using individualized and specific dental procedures.