Coats' disease, Turner syndrome, and von Willebrand disease in a patient with Wildtype Norrie disease pseudoglioma

Rajen U. Desai, Norman A. Saffra, Rati P. Krishna, Steven E. Rosenberg

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

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 languageEnglish
Pages (from-to)e1-e3
JournalJournal of Pediatric Ophthalmology and Strabismus
Volume48 Online
DOIs
StatePublished - 2011

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