Keywords
Congenital Horner’s syndrome Heterochromia iridisNotes
Conflict of interest
On behalf of all authors, the corresponding author states that there is no conflict of interest.
Ethical standard
This article does not contain any studies with human participants performed by any of the authors.
Informed consent
Informed consent was obtained from all individual participants included in the study.
References
- 1.Jeffery AR, Ellis FJ, Repka MX, Buncic R (1998) Pediatric Horner syndrome. J AAPOS 2:159–167CrossRefPubMedGoogle Scholar
- 2.Morrison DA, Bibby K, Woodruff G (1997) The “Harlequin” sign and congenital Horner’s syndrome. J Neurol Neurosurg Psychiatry 62:626–628PubMedCentralCrossRefPubMedGoogle Scholar
- 3.Ur Rehman H (2008) Heterochromia. CMAJ 179:447–448PubMedCentralCrossRefGoogle Scholar
- 4.Robinson GC, Dikrainian DA, Roseborough GF (1965) Congenital Horner’s syndrome and heterochromia iridum: their association with congenital foregut and vertebral anomalies. Pediatrics 35:103–107PubMedGoogle Scholar
- 5.Hageman G, Ippel PF, te Nijenhuis FCAM (1992) Autosomal dominant congenital Horner’s syndrome in a Dutch family. J Neurol Neurosurg Psychiatry 55:28–30PubMedCentralCrossRefPubMedGoogle Scholar
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© Belgian Neurological Society 2015