Abstract
The authors describe a girl diagnosed as having Coats' disease, Turner syndrome (45X karyotype), and type 1 von Willebrand disease. She tested negative for the Norrie disease pseudoglioma (NDP) gene located on the X-chromosome, which has been suspected of contributing to Coats' disease.
Original language | English |
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Pages (from-to) | e1-e3 |
Journal | Journal of Pediatric Ophthalmology and Strabismus |
Volume | 48 Online |
DOIs | |
State | Published - 2011 |