Urs Aadithya B, Augustine Jeyaseelan, Khan Azhar Ahmed
Department of Oral and Maxillofacial Pathology, Maulana Azad Institute of Dental Sciences, New Delhi, India.
Contemp Clin Dent. 2021 Jan-Mar;12(1):73-75. doi: 10.4103/ccd.ccd_207_20. Epub 2021 Mar 20.
Chorea-acanthocytosis (ChAc) is an autosomal recessive, progressive neurological disorder due to mutation in VPS13A gene causing defects in sorting of protein making the cell membrane unstable, leading to star-shaped erythrocytes. This neurological disorder includes features such as elevated creatinine kinase, atrophy of basal ganglia, and oral manifestations such as frequent cheek and tongue biting. It is a rare neurological condition with an estimate of <1000 cases worldwide. A case of 47-year-old male patient with a history of seizures and neurological problems presenting with oral ulceration has been discussed. The diagnosis of ChAc was confirmed by molecular investigations showing VPS13A gene mutation. The physical appearance includes chorea and dystonia with impaired gait. We attempt to highlight the oral features of ChAc. The oral manifestations include frequent tongue and cheek biting occurring due to dystonia affecting the muscles of head and neck region.
舞蹈病-棘红细胞增多症(ChAc)是一种常染色体隐性进行性神经障碍,由VPS13A基因突变引起,该突变导致蛋白质分选缺陷,使细胞膜不稳定,进而产生星形红细胞。这种神经障碍包括肌酸激酶升高、基底神经节萎缩等特征,以及频繁咬颊和咬舌等口腔表现。它是一种罕见的神经疾病,全球估计病例数不足1000例。本文讨论了一例47岁男性患者,有癫痫发作和神经问题病史,现出现口腔溃疡。通过分子检测显示VPS13A基因突变,确诊为ChAc。其身体表现包括舞蹈症和肌张力障碍,步态受损。我们试图突出ChAc的口腔特征。口腔表现包括由于影响头颈部肌肉的肌张力障碍而频繁咬舌和咬颊。