Ye, Yuhong
Wang, Jingjing
Quan, Xiaofang
Xu, Ke
Fu, Haidong
Gu, Weiyue
Mao, Jianhua
Funding for this research was provided by:
National Natural Science Foundation of China (81470939& 81770710)
Specialized Research Fund for the Doctoral Program of Higher Education of China (20120101110018)
Natural Science Foundation of Zhejiang Province (LH14H050002&LY15H050001)
Medicine & Health Technology Innovation Project of Zhejiang Province (2014KYA123)
Article History
Received: 27 September 2019
Accepted: 22 April 2020
First Online: 11 May 2020
Ethics approval and consent to participate
: The parents, who are legal guardians, of the patient had been informed about the availability and importance of genetic tests, including DNA and karyotyping, and the parents contented to the use of the anonymized test results and de-identified health information as described in this article.
: Written informed consent was obtained from the patient’s parents for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
: The authors declare that they have no competing interests.