论文部分内容阅读
锁骨颅骨发育不全症是一种罕见的牙颌及骨髂系统发育畸形。1760年Meckel首先报告一例婴儿生后没有锁骨。1946年Soule曾收集世界各地所发表的本症文献,总计有323例。其中198例显示有遗传性,125例遗传因素不明。我国1954年由冯亮首先报告一例本症患者,其遗传因素不明。1958年高柠等报告一个家族中有多例本症患者,显示有遗传性。1986年赵文川等报告本症一例。我院于1987年2月7日诊治本症一例,现报告如下。病例报告患者赵某某、男、15岁、朝鲜族、学生。因咀嚼功能不良前来就诊。该患者系第二胎足月顺产。其祖母、父、母及姐、弟均健康,无类似发病。
Cranial dysplasia of the skull is a rare dental and bony iliac system deformity. In 1760 Meckel first reported a case of baby clavicle after birth. In 1946, Soule collected a total of 323 cases of the disease published in the world. 198 cases showed hereditary, 125 cases of unknown genetic factors. In 1954, Feng Liang first reported a case of our patient with unknown genetic factors. 1958 Gao Le reported a family of patients with multiple patients with the disease, showing hereditary. Zhao Wenchuan 1986 report of a case of this disease. Our hospital in February 7, 1987 diagnosis and treatment of a case of disease, are as follows. Case report Zhao Moumou, male, 15 years old, Korean, student. For chewing dysfunction came to see a doctor. The patient was born on a second full-term follow-up. His grandmother, father, mother and sister, brother are healthy, no similar incidence.