Friedman J M
Department of Medical Genetics at the University of British Columbia and Children's and Women's Health Centre of British Columbia, Vancouver, Canada.
Am J Med Genet. 1999 Mar 26;89(1):1-6.
The prevalence of neurofibromatosis type 1 (NF1) is about 1/3,000. There are no known ethnic groups in which NF1 does not occur or is unusually common. The prevalence is somewhat higher in young children than in adults, a difference that probably results at least in part from the early death of some NF1 patients. NF1 is fully penetrant in adults, but many disease features increase in frequency or severity with age. The reproductive fitness of NF1 patients is reduced by about one-half. About half of all cases result from new mutations. The estimated rate of new NF1 mutations is unusually high, but the basis for this high mutation rate is not known. Am. J. Med. Genet. (Semin. Med. Genet.) 89:1-6, 1999.
1型神经纤维瘤病(NF1)的患病率约为1/3000。不存在NF1不发生或异常常见的已知种族群体。幼儿中的患病率略高于成人,这种差异可能至少部分是由于一些NF1患者过早死亡所致。NF1在成年人中具有完全的外显率,但许多疾病特征的频率或严重程度会随着年龄的增长而增加。NF1患者的生殖适应性降低了约一半。所有病例中约一半是由新突变引起的。新的NF1突变估计率异常高,但这种高突变率的原因尚不清楚。《美国医学遗传学杂志》(医学遗传学研讨会)89:1 - 6,1999年。