Alamankany Abeer
Department of Pediatric Dentistry, Taibah University, Medina, Saudi Arabia.
Int J Health Sci (Qassim). 2021 Jan-Feb;15(1):56-58.
A 16-month-old Saudi boy has microcephaly and three rare genetic diseases [Riga Fede disease (RFD), Niemann-Pick C disease, and Fabry disease. In the published literature, there is no reported case with these four associations, especially RFD affection of the dorsal surface of the tongue. It is also a clear demonstration of how the proper diagnosis and treatment could provide a better quality of life, ease pain, resources, and money saving. The difficult RDF ulcer was resolved by a conservative treatment, which was accomplished by smoothing sharp edges and removing mamelons of the lower primary incisors using a diamond bur in a high-speed dental handpiece. The aim of this report is to present and discuss steps of diagnosis and the effect of misdiagnosis on the management of a very rare case.
一名16个月大的沙特男孩患有小头畸形和三种罕见的遗传疾病[里加-费德病(RFD)、尼曼-匹克C病和法布里病]。在已发表的文献中,没有这四种病症同时出现的报道病例,尤其是舌背受RFD影响的情况。这也清楚地表明了正确的诊断和治疗如何能够提供更好的生活质量、减轻疼痛、节省资源和金钱。通过保守治疗解决了棘手的RDF溃疡,具体做法是使用高速牙科手机上的金刚砂车针磨平下乳切牙的尖锐边缘并去除牙乳头。本报告的目的是介绍和讨论诊断步骤以及误诊对这一罕见病例治疗的影响。