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. 2017 Sep 22;96(38):e8068. doi: 10.1097/MD.0000000000008068

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Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-nc-sa/4.0

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Pedigree of a Chinese family affected with CFEOM1. Normal individuals are shown as empty symbols. Affected males and females are indicated by filled-in squares and circles, respectively. The proband of the pedigree is indicated by an arrow. Deceased individuals are indicated by a slash (/). The normal individual who lost contact with her family at 4 years old is indicated by a question mark (?). The affected male who was unable to be examined due to his occupation as a migrant worker is indicated by octothorpe (#). CFEOM1 = congenital fibrosis of the extraocular muscles type 1.