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。

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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。

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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。

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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。

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