Macrocephaly associated with the DICER1 syndrome

被引:42
作者
Khan, Nicholas E. [1 ]
Bauer, Andrew J. [2 ]
Doros, Leslie [3 ]
Schultz, Kris Ann P. [4 ,5 ,6 ]
Decastro, Rosamma M. [1 ]
Harney, Laura A. [7 ]
Kase, Ron G. [7 ]
Carr, Ann G. [7 ]
Harris, Anne K. [4 ,5 ,6 ]
Williams, Gretchen M. [4 ,5 ]
Dehner, Louis R. [8 ]
Messinger, Yoav H. [4 ,5 ]
Stewart, Douglas R. [1 ]
机构
[1] NCI, Clin Genet Branch, Div Canc Epidemiol & Genet, Rockville, MD 20850 USA
[2] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[3] Childrens Natl Med Ctr, Washington, DC 20010 USA
[4] Childrens Hosp & Clin Minnesota, Minneapolis, MN USA
[5] Int Pleuropulm Blastoma Registry, Minneapolis, MN USA
[6] Int Ovarian & Testicular Stromal Tumor Registry, Minneapolis, MN USA
[7] Westat Corp, Rockville, MD USA
[8] Washington Univ, St Louis, MO USA
关键词
DICER1; macrocephaly; PLEUROPULMONARY BLASTOMA; MUTATIONS; GERMLINE;
D O I
10.1038/gim.2016.83
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: Germ-line mutations in DICER1 increase the risk cif various tumors, including pleuropulmonary blastoma. Macrocephaly and symmetric overgrowth have been reported in some, but not all, patients with mosaic DICER1 RNase Mb mutations. The prevalence of these features in individuals with constitutional germ-line DICERI mutations is unknown. Methods: 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. Results: 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 rhacrocephalic (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. Conclusion: 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.
引用
收藏
页码:244 / 248
页数:5
相关论文
共 20 条
[1]  
[Anonymous], 2014, GENEREVIEWS
[2]  
Brenneman Mark, 2015, F1000Res, V4, P214, DOI 10.12688/f1000research.6746.1
[3]   CENTILES FOR ADULT HEAD CIRCUMFERENCE [J].
BUSHBY, KMD ;
COLE, T ;
MATTHEWS, JNS ;
GOODSHIP, JA .
ARCHIVES OF DISEASE IN CHILDHOOD, 1992, 67 (10) :1286-1287
[4]   High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndrome [J].
de Kock, Leanne ;
Wang, Yu Chang ;
Revil, Timothee ;
Badescu, Dunarel ;
Rivera, Barbara ;
Sabbaghian, Nelly ;
Wu, Mona ;
Weber, Evan ;
Sandoval, Claudio ;
Hopman, Saskia M. J. ;
Merks, Johannes H. M. ;
van Hagen, Johanna M. ;
Bouts, Antonia H. M. ;
Plager, David A. ;
Ramasubramanian, Aparna ;
Forsmark, Linus ;
Doyle, Kristine L. ;
Toler, Tonja ;
Callahan, Janine ;
Engelenberg, Charlotte ;
Bouron-Dal Soglio, Dorothee ;
Priest, John R. ;
Ragoussis, Jiannis ;
Foulkes, William D. .
JOURNAL OF MEDICAL GENETICS, 2016, 53 (01) :43-52
[5]  
Dishop MK, 2008, ARCH PATHOL LAB MED, V132, P1079, DOI 10.1043/1543-2165(2008)132[1079:PAMLTI]2.0.CO
[6]  
2
[7]  
Gripp K. W., 2013, Handbook of Physical Measurements, V3
[8]  
Gutmann D.H., 1999, Neurofibromatosis: Phenotype, Natural History, and Pathogenesis, VThird, P190
[9]   DICER1 Mutations in Familial Pleuropulmonary Blastoma [J].
Hill, D. Ashley ;
Ivanovich, Jennifer ;
Priest, John R. ;
Gurnett, Christina A. ;
Dehner, Louis P. ;
Desruisseau, David ;
Jarzembowski, Jason A. ;
Wikenheiser-Brokamp, Kathryn A. ;
Suarez, Brian K. ;
Whelan, Alison J. ;
Williams, Gretchen ;
Bracamontes, Dawn ;
Messinger, Yoav ;
Goodfellow, Paul J. .
SCIENCE, 2009, 325 (5943) :965-965
[10]   Expanding the phenotype of mutations in DICER1: mosaic missense mutations in the RNase IIIb domain of DICER1 cause GLOW syndrome [J].
Klein, Steven ;
Lee, Hane ;
Ghahremani, Shahnaz ;
Kempert, Pamela ;
Ischander, Mariam ;
Teitell, Michael A. ;
Nelson, Stanley F. ;
Martinez-Agosto, Julian A. .
JOURNAL OF MEDICAL GENETICS, 2014, 51 (05) :294-302