Other Names for this Disease
- Bernard-Horner Syndrome
- Oculosympathetic Palsy
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ptosis (drooping of the upper eyelid), and anhidrosis (absence of sweating of the face). It is caused by injury to the sympathetic nerves of the face. In rare cases, Horner's syndrome is congenital (present from birth) and associated with a lack of pigmentation of the iris (colored part of the eye).Horner's syndrome consists of miosis (constriction of the pupil),
Last updated: 10/1/2014
- Horner syndrome. MedlinePlus. May 20, 2014; http://www.nlm.nih.gov/medlineplus/ency/article/000708.htm. Accessed 10/1/2014.
- Horner's syndrome. National Organization for Rare Disorders (NORD). 2003; http://www.rarediseases.org/rare-disease-information/rare-diseases/byID/864/viewAbstract. Accessed 10/1/2014.
- Rolf Salvesen. Horner Syndrome. NORD Guide to Rare Disorders. Philadelphia, PA: Lippincott Williams & Wilkins; 2003;
- Genetics Home Reference contains information on Horner's syndrome. This website is maintained by the National Library of Medicine.
- MayoClinic.com offers additional information about Horner syndrome. Click on the above link to access this information.
- MedlinePlus was designed by the National Library of Medicine to help you research your health questions, and it provides more information about this topic.
- The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.
- Medscape Reference provides information on this topic. You may need to register to view the medical textbook, but registration is free.
- The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
- 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.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Horner's syndrome. Click on the link to view a sample search on this topic.