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Xu, C. Horner Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/4120 (accessed on 26 September 2026).
Xu C. Horner Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/4120. Accessed September 26, 2026.
Xu, Camila. "Horner Syndrome" Encyclopedia, https://encyclopedia.pub/entry/4120 (accessed September 26, 2026).
Xu, C. (2020, December 23). Horner Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/4120
Xu, Camila. "Horner Syndrome." Encyclopedia. Web. 23 December, 2020.
Horner Syndrome
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/horner-syndrome

Horner syndrome is a disorder that affects the eye and surrounding tissues on one side of the face and results from paralysis of certain nerves.

genetic conditions

References

  1. Fons C, Vasconcelos M, Vidal M, Puy R, Capdevila A, Sanchez L, Campistol J.Agenesis of internal carotid artery in a child with ipsilateral Horner'ssyndrome. J Child Neurol. 2009 Jan;24(1):101-4. doi: 10.1177/0883073808321049.Review.
  2. Jeffery AR, Ellis FJ, Repka MX, Buncic JR. Pediatric Horner syndrome. J AAPOS.1998 Jun;2(3):159-67.
  3. Mahoney NR, Liu GT, Menacker SJ, Wilson MC, Hogarty MD, Maris JM. Pediatrichorner syndrome: etiologies and roles of imaging and urine studies to detectneuroblastoma and other responsible mass lesions. Am J Ophthalmol. 2006Oct;142(4):651-9.
  4. Renard D, Jeanjean L, Labauge P. Heterochromia Iridis in congenital Horner'ssyndrome. Eur Neurol. 2010;63(4):253. doi: 10.1159/000276946.
  5. Smith SJ, Diehl N, Leavitt JA, Mohney BG. Incidence of pediatric Hornersyndrome and the risk of neuroblastoma: a population-based study. ArchOphthalmol. 2010 Mar;128(3):324-9. doi: 10.1001/archophthalmol.2010.6.
  6. Walton KA, Buono LM. Horner syndrome. Curr Opin Ophthalmol. 2003Dec;14(6):357-63. Review.
  7. Wang FM, Wertenbaker C, Cho H, Marmor MA, Ahn-Lee SS, Bernard BA. Unilateralstraight hair and congenital horner syndrome. J Neuroophthalmol. 2012Jun;32(2):132-4. doi: 10.1097/WNO.0b013e318240c678.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Camila Xu
View Times: 1.0K
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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