Rizos M, Negrón R J, Serman N
Department of Orthodontics, Columbia University, New York, New York, USA.
Cleft Palate Craniofac J. 1998 May;35(3):262-8. doi: 10.1597/1545-1569_1998_035_0262_mbswdi_2.3.co_2.
The clinicopathological findings on a 17-year-old female with the Möbius/Moebius syndrome are reported. The signs and symptoms of this neuromuscular condition include congenital bilateral or unilateral palsies of the facial and abducens cranial nerves and a broad scope of multisystem abnormalities. A case of unilateral deficiencies of cranial nerves VI and VII, congenital ectrodactyly of toes, and multiple congenitally missing primary and permanent teeth is reported. A review of the literature reveals various ideas regarding the diversity of symptoms and the etiology of the syndrome. The purpose of this article is to report oral manifestations, such as congenitally missing teeth, associated with Möbius syndrome.
报告了一名患有莫比乌斯综合征的17岁女性的临床病理结果。这种神经肌肉疾病的体征和症状包括先天性双侧或单侧面神经和展神经麻痹，以及广泛的多系统异常。报告了一例单侧第六和第七颅神经缺陷、先天性足趾缺指（趾）畸形以及多颗先天性恒牙和乳牙缺失的病例。文献综述揭示了关于该综合征症状多样性和病因的各种观点。本文的目的是报告与莫比乌斯综合征相关的口腔表现，如先天性缺牙。
