17p13.3 microduplication including CRK leads to overgrowth and elevated growth factors: A case report

被引:8
|
作者
Henry, Rohan K. [1 ]
Astbury, Caroline [2 ,3 ]
Stratakis, Constantine A. [4 ]
Hickey, Scott E. [5 ]
机构
[1] Ohio State Univ, Coll Med, Nationwide Childrens Hosp, Div Endocrinol,Dept Pediat, Columbus, OH 43205 USA
[2] Nationwide Childrens Hosp, Dept Pathol & Lab Med, Columbus, OH USA
[3] Ohio State Univ, Coll Med, Dept Pathol, Columbus, OH 43210 USA
[4] NICHHD, Dev Endocrinol & Genet, NICHD, NIH, Bethesda, MD 20892 USA
[5] Ohio State Univ, Coll Med, Nationwide Childrens Hosp, Div Mol & Human Genet,Dept Pediat, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
17p13.3; microduplications; CRK gene; Growth factors; Central precocious puberty; RECEPTOR TYROSINE KINASE; I RECEPTOR; C-CRK; HYPERPLASIA; DELINEATION; PHENOTYPES;
D O I
10.1016/j.ejmg.2016.09.006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
17p13.3 microduplications classified as class I duplications involving YWHAE but not PAFAH1B1 (formerly LIS1) and class II duplications which extend to involve PAFAH1B1, are associated with diverse phenotypes including intellectual disability and structural brain malformations. We report a girl with an approximately 1.58 Mb apparently terminal gain of 17p13.3, which contains more than 20 genes including the YWHAE and CRK genes (OMIM: 164762). She had increased growth factors accompanied by pathologic tall stature. In addition to these, she developed central precocious puberty at 7 years old. In individuals with class I 17p13.3 microduplications including CRK, we recommend biochemical evaluation of the growth hormone axis. Providers caring for these patients should be aware of their possible risk for the development of central precocious puberty. (C) 2016 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:512 / 516
页数:5
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