Other Names for this Disease
- Congenital microcoria
- Congenital miosis
- Miosis, congenital
- Pinhole pupils
pupils of less than 2 mm diameter and is caused by the underdevelopment of the dilator pupillae muscle of the iris. This anomaly is associated with nearsightedness and glaucoma.Congenital microcoria is a rare anomaly of the pupils. It is characterized by
Last updated: 7/19/2013
- Rouillac C, Roche O, Marchant D, Bachner L, Kobetz A, Toulemont PJ, Orssaud C, Urvoy M, Odent S, Le Marec B, Abitbol M, Dufier JL. Mapping of a Congenital Microcoria Locus to 13q31-q32. Am. J. Hum. Genet. 1998;
- Ramprasad VL, Sripriya S, Ronnie G, Nancarrow D, Saxena S, Hemamalini A, Kumar D, Vijaya L, Kumaramanickavel G. Molecular Vision. 2005; http://www.molvis.org/molvis/v11/a112/. Accessed 3/17/2008.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Microcoria, congenital. Click on the link to view a sample search on this topic.
- A diagram of the eye can be found by visiting MedlinePlus, the National Library of Medicine Web site designed to help you research your health questions. Click on MedlinePlus to view the diagram.