| Literature DB >> 24666291 |
Nurgül Örnek1, Reyhan Oğurel1, Kemal Örnek1.
Abstract
Rieger syndrome (RS) is a multiple malformation syndrome characterized by ocular manifestations and extraocular defects. Herein, we report a 9-year-old boy who exhibited Rieger Syndrome phenotype as well as congenital hypothyroidism which may be an underappreciated feature of RS.Entities:
Keywords: Congenital; Rieger Syndrome; hypothyroidism
Mesh：
Substances：
Year: 2014 PMID： 24666291 DOI： 10.3109/13816810.2014.902079
Source DB: PubMed Journal: Ophthalmic Genet ISSN： 1381-6810 Impact factor: 1.803