Objective to detect the mutation on exons 32, 33 of Chinese the neurofibromatosis type 1 (NF1) gene.
目的检测中国人神经纤维瘤病1型(nf1)基因32、33外显子突变。
Objective To investigate the growth characteristic, clinical manifestations, diagnosis and treatment of neurofibromatosis type 1 (NF1) in oral and maxillofacial regions for the better curative effect.
目的探讨Ⅰ型神经纤维瘤病的临床表现、诊断、治疗，为临床积累经验，提高治疗效果。
Sphenoid wing dysplasia can occur as an isolated finding or in patients who have Neurofibromatosis type 1. Approximately 50% of cases are associated with neurofibromatosis type 1.
蝶骨翼发育不良可以是一个孤立性的发现，也可以见于神经纤维瘤病I型患者。
Recent studies indicate that patients with type I neurofibromatosis usually have osteopenia or osteoporosis.
最近研究表明I型神经纤维瘤病患者常表现出不同程度的骨量减少或骨质疏松。
Recent studies indicate that patients with type I neurofibromatosis usually have osteopenia or osteoporosis.
最近研究表明I型神经纤维瘤病患者常表现出不同程度的骨量减少或骨质疏松。
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