Kim Young Ho, Roh Dong Hwan, Choi Byung Yoon, Oh Seung-Ha
Departments of Otolaryngology-Head & Neck Surgery, Seoul Municipal Boramae Hospital, Seoul, South Korea.
Acta Otolaryngol. 2005 Jul;125(7):797-800. doi: 10.1080/00016480510028474.
Craniometaphyseal dysplasia is a rare bone disorder of unknown etiology characterized by overgrowth of the skull base or craniofacial bones and abnormal remodeling of the metaphyses of the long bones. We present a sporadic case of craniometaphyseal dysplasia associated with facial paralysis observed in a 4-year-old female, which emphasizes the importance of the early detection of accompanying lesions.
颅骨干骺端发育异常是一种病因不明的罕见骨骼疾病,其特征为颅底或颅面骨过度生长以及长骨干骺端异常重塑。我们报告了一例4岁女性散发性颅骨干骺端发育异常伴面瘫的病例,该病例强调了早期发现伴随病变的重要性。