Children (Aug 2024)

First Description of a Large Clinical Series of Fetal Alcohol Spectrum Disorders Children and Adolescents in Reunion Island, France

  • Laëtitia Sennsfelder,
  • Susie Guilly,
  • Sonia Henkous,
  • Christophe Lebon,
  • Sébastien Leruste,
  • Pauline Beuvain,
  • Fanny Ferroul,
  • Stéphanie Benard,
  • Frédérique Payet,
  • Meissa Nekaa,
  • Maité Bagard,
  • Magaly Lauret,
  • Virginie Hoareau,
  • Aurélie Caillier,
  • Stéphanie Robin,
  • Justine Lanneaux,
  • Léa Etchebarren,
  • Michel Spodenkiewicz,
  • Jean-Luc Alessandri,
  • Godelieve Morel,
  • Bérénice Roy-Doray

DOI
https://doi.org/10.3390/children11080955
Journal volume & issue
Vol. 11, no. 8
p. 955

Abstract

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Background: Despite several diagnostic guidelines, Fetal Alcohol Spectrum Disorders (FASDs) remain underdiagnosed or misdiagnosed, delaying the care of these patients and support for families. Objective: This study aims to help professionals caring for these children and their families to suspect this diagnosis earlier and to provide the most appropriate follow-up. Methods: A retrospective chart review with monocentric recruitment was performed at the Genetics Unit of the University Hospital of Reunion Island. A total of 147 children and adolescents with FASDs were included. Results: Prenatal alcohol exposure was associated with paternal alcohol consumption in 42.9%, and a high rate of prematurity (33.3%) was observed. Sixty percent of children or adolescents were placed in foster families. Learning difficulties without cognitive deficits were found in 65.8% of cases (50/76). Postural control and fine motor skills disabilities were described, respectively, in 54.7% (35/64) and 72.5% (50/69) of cases. A systematic genetic assessment was carried out, identifying in these FASD patients an associated Copy Number Variation (CNVs) in 22.6% of cases. Conclusion: Children with FASDs combine significant vulnerabilities, associating exposure to alcohol during the preconception and/or the prenatal period, prematurity, complex familial and sociocultural living conditions, and a genetic anomaly in almost a quarter of cases.

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