129: Diagnosing Fetal Alcohol Spectrum Disorder, the Need for Genetic Testing: A Pilot Study. Issue 6 (1st June 2014)

• Record Type: Journal Article
• Authors: Stade, BC; Watson, W; Bonifacio, J; McCleod, HJ; Barozzino, T; DiMarchi, A; Becker, B; Bartholomew, L; Sgro, M
• Is Part Of: Paediatrics & Child Health. Volume 19:Issue 6(2014)
• Page Start: e80
• Page End: e81
• Publication Date: 2014-06-01
• Subjects: Pediatrics -- Periodicals; Children -- Health and hygiene -- Periodicals; 618.92
• DOI: 10.1093/pch/19.6.e35-127
• Languages: English
• ISSNs: 1205-7088

Abstract

Abstract: BACKGROUND: Fetal Alcohol Spectrum Disorder (FASD) has no specific diagnostic marker, and the facial features and growth restriction found in the full Fetal Alcohol Syndrome are found only in a small percentage of children diagnosed within the Fetal Alcohol Spectrum. The presentation of FASD often overlaps with genetic syndromes. Thus, a genetic opinion is frequently requested in the assessment of a child with suspected FASD. OBJECTIVES: To study the outcome of genetic assessments of 220 children and youth referred to a FASD clinic between 2009 and 2013. DESIGN/METHODS: DESIGN: Prospective study design. PARTICIPANTS: 220 children and youth, aged 18 months to 23 years. SETTING: FASD clinic in a large teaching hospital in Ontario. METHODS: Data from the medical records were abstracted, entered onto a standard study pro forma, recorded in an Excel spreadsheet, and analyzed using simple frequency analysis. RESULTS: Sixty-eight percent of children and youth assessed in the clinic were diagnosed with Fetal Alcohol Spectrum Disorder. Twenty-eight percent had at least one facial feature of the full Fetal Alcohol Syndrome including thin upper lip, smooth philtrum, or short palpebral fissures. Only 4% had all of the three facial features. The most common alternative diagnosis was a chromosome disorder including Fragile X, 22q11.2 deletion, Williams Syndrome and others, representing 11.2% of the FASD referrals. CONCLUSIONS: Genetic assessment was of particular value in excluding other diagnoses and providing information to caregivers. Structural malformations were not common in the group overall, and some previously reported diagnostic signs were not found to be reliable markers of FASD. Chromosome disorders showed phenotypic overlap with FASD, and are an important differential diagnosis. The study findings support a large multi-centre project.