“…Previous studies on oral manifestations in paediatric allogeneic bone marrow transplant recipients. Previous have reported on oral complications in patients following allogeneic HSCT (Bhatt et al, 2022;Bollero et al, 2018;Sholkamy et al, 2022;Tanem et al, 2022;Vignon et al, 2017), though the oral health in paediatric HSCT survivors has rarely been described (Chow et al, 2016;Effinger et al, 2014;Nicolatou-Galitis et al, 2001;Treister et al, 2005). Boer et al showed that oral mucosal cGVHD was the most common finding post-allogeneic HSCT (n = 35; 55.7%) in their cohort of patients, followed by xerostomia and pain (n = 34; 98.7%), mouth pain (n = 18; 29.5%) and difficulty in swallowing (n = 8; 13.1%), respectively (Boer et al, 2010).…”