Avoidant-restrictive food intake disorder in a male patient with Goldenhar syndrome

被引:4
作者
Bergonzini, Luca [1 ,2 ]
Pruccoli, Jacopo [1 ,2 ]
Parmeggiani, Antonia [1 ,2 ]
机构
[1] IRCCS Ist Sci Neurol Bologna, UO Neuropsichiatria Eta Pediat, Ctr Reg & Disturbi Nutr & Alimentaz Eta Evolut, Bologna, Italy
[2] Univ Bologna, Dipartimento Sci Med & Chirurg DIMEC, Bologna, Italy
关键词
Goldenhar syndrome; Avoidant; restrictive food intake disorder; Children and adolescents; Pediatric; SPECTRUM;
D O I
10.1007/s40519-022-01497-1
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background Goldenhar syndrome (GS) is a rare congenital condition characterized by the underdevelopment of structures deriving from the first and second branchial arches. Clinical phenotype might encompass extra-craniofacial abnormalities, and patients may experience neuropsychiatric disorders with a higher prevalence than healthy controls. To the best of our knowledge, an association between GS and Feeding and Eating Disorders (FED) has never been reported in the literature. Case report A 15-year-old boy with GS was referred to our outpatient clinic due to severe underweight (BMI of 12.7 kg/m(2)) and food intake disorder with avoidant restrictive features. After a diagnosis of avoidant-restrictive food intake disorder (ARFID) was made, an inpatient multidisciplinary intervention and outpatient follow-up program were provided, which resulted in the improvement of the boy's weight and FED psychopathology. Conclusions The current report describes the first case of a young male with GS and ARFID. We suggest that ARFID may present itself as part of the spectrum of neuropsychiatric disorders associated with the syndrome; since traumatic experiences and gastrointestinal discomfort play a pivotal role in the development of ARFID among children, attention should be paid to those affected by GS that involves crucial structures in the swallowing process. Further literature evidence will help portray the complex relationship between ARFID and GS more precisely.
引用
收藏
页码:3803 / 3807
页数:5
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