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      Interventions in fetal alcohol spectrum disorders: An international perspective

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      European Journal of Medical Genetics
      Elsevier BV

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          A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010

          The Lancet, 380(9859), 2224-2260
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            Fetal alcohol spectrum disorder: Canadian guidelines for diagnosis.

            The diagnosis of fetal alcohol spectrum disorder (FASD) is complex and guidelines are warranted. A subcommittee of the Public Health Agency of Canada's National Advisory Committee on Fetal Alcohol Spectrum Disorder reviewed, analysed and integrated current approaches to diagnosis to reach agreement on a standard in Canada. The purpose of this paper is to review and clarify the use of current diagnostic systems and make recommendations on their application for diagnosis of FASD-related disabilities in people of all ages. The guidelines are based on widespread consultation of expert practitioners and partners in the field. The guidelines have been organized into 7 categories: screening and referral; the physical examination and differential diagnosis; the neurobehavioural assessment; and treatment and follow-up; maternal alcohol history in pregnancy; diagnostic criteria for fetal alcohol syndrome (FAS), partial FAS and alcohol-related neurodevelopmental disorder; and harmonization of Institute of Medicine and 4-Digit Diagnostic Code approaches. The diagnosis requires a comprehensive history and physical and neurobehavioural assessments; a multidisciplinary approach is necessary. These are the first Canadian guidelines for the diagnosis of FAS and its related disabilities, developed by broad-based consultation among experts in diagnosis.
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              Fetal alcohol spectrum disorder: a guideline for diagnosis across the lifespan.

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                Author and article information

                Journal
                European Journal of Medical Genetics
                European Journal of Medical Genetics
                Elsevier BV
                17697212
                January 2017
                January 2017
                : 60
                : 1
                : 79-91
                Article
                10.1016/j.ejmg.2016.10.005
                5205562
                27742482
                880d0cb6-c232-4ed2-af18-323c736f1f82
                © 2017
                History

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