Khan Nicholas E, Bauer Andrew J, Doros Leslie, Schultz Kris Ann P, Decastro Rosamma M, Harney Laura A, Kase Ron G, Carr Ann G, Harris Anne K, Williams Gretchen M, Dehner Louis P, Messinger Yoav H, Stewart Douglas R
Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Genet Med. 2017 Feb;19(2):244-248. doi: 10.1038/gim.2016.83. Epub 2016 Jul 21.
Germ-line mutations in DICER1 increase the risk of various tumors, including pleuropulmonary blastoma. Macrocephaly and symmetric overgrowth have been reported in some, but not all, patients with mosaic DICER1 RNase IIIb mutations. The prevalence of these features in individuals with constitutional germ-line DICER1 mutations is unknown.
We analyzed prospectively collected auxology data from 67 DICER1 mutation carriers and 43 family controls. We assessed differences between groups using an exact test for proportions and generalized estimating equations for continuous dependent variables.
Twenty-eight DICER1 mutation carriers (42%) were macrocephalic, and none had an occipitofrontal circumference (OFC) below the third centile, which significantly differed from family controls, of whom five were macrocephalic (12%) and two had OFC below the third centile (5%) (P < 0.001). DICER1 mutation carriers were taller than familial controls after controlling for gender (P = 0.048), but similar proportions of both groups were above the 97th centile of population norms. Head circumference remained increased after adjusting for differences in height.
For the first time, we establish macrocephaly as a common finding in the DICER1 syndrome. Like some other tumor-predisposition disorders, macrocephaly may be a useful, albeit a subtle, clinical clue to the DICER1 syndrome diagnosis.Genet Med 19 2, 244-248.
DICER1基因的种系突变会增加包括胸膜肺母细胞瘤在内的多种肿瘤的发病风险。在部分(而非全部)携带DICER1核糖核酸酶IIIb镶嵌突变的患者中,曾有巨头畸形和对称性过度生长的报道。而在携带DICER1基因种系突变的个体中,这些特征的发生率尚不清楚。
我们对前瞻性收集的67例DICER1突变携带者和43例家族对照的生长学数据进行了分析。我们使用比例精确检验和连续因变量的广义估计方程来评估组间差异。
28例DICER1突变携带者(42%)有巨头畸形,且枕额周长(OFC)均未低于第三百分位数,这与家族对照有显著差异,家族对照中有5例(12%)有巨头畸形,2例(5%)OFC低于第三百分位数(P<0.001)。在控制性别因素后,DICER1突变携带者比家族对照更高(P=0.048),但两组中高于人群标准第97百分位数的比例相似。在对身高差异进行调整后,头围仍偏高。
我们首次证实巨头畸形是DICER1综合征的常见表现。与其他一些肿瘤易感疾病一样,巨头畸形可能是诊断DICER1综合征的一个有用的临床线索,尽管较为细微。《基因医学》第19卷第2期,第244 - 248页