Co-existence of Beckwith-Wiedemann syndrome and autism spectrum disorder
Künye
Alnak, A., Bulanik Ozdemirci, D., & Coskun, M. (2019). Co-existence of Beckwith-Wiedemann syndrome and autism spectrum disorder. Dusunen Adam The Journal of Psychiatry and Neurological Sciences, 32(3), 268.Özet
Autism spectrum disorder (ASD) is an early-onset neurodevelopmental disorder characterized by deficits in communicative
and social skills and repetitive behaviors and/or restricted interests. The genetic mechanism underlying ASD is as complex and
heterogeneous as its clinical heterogeneity. Beckwith-Wiedemann syndrome (BWS) is a well-known human imprinting disorder
characterized by macroglossia, visceromegaly, hemihypertrophy, abdominal wall defects and a number of other various
developmental abnormalities with an increased risk for embryonal tumors. In the literature, a greater frequency of
neurobehavioral issues including ASD has been reported in children with BWS. Here, we present a 7-year-old boy diagnosed
with ASD and BWS admitted to our clinic with complaints of emotional and behavioral changes after suddenly losing his father
due to myocardial infarction. Upon initial assessment and psychiatric examination, the ASD diagnosis was confirmed and the
exacerbation of the symptoms was assumed to be related with his bereavement. The family was given psychoeducation and
the boy was started on escitalopram 0.5 mg/day, gradually increased to 2.5 mg/day. One month after this intervention, the
family reported significant improvements in his symptoms. Although BWS has not been studied as extensively as other genetic
conditions associated with neurodevelopmental disorders, it may be important for us to expand our knowledge about ASD
accompanying human imprinting diseases including BWS.