Cargando…
Congenital Horner Syndrome with Heterochromia Iridis Associated with Ipsilateral Internal Carotid Artery Hypoplasia
BACKGROUND: Horner syndrome (HS), also known as Claude-Bernard-Horner syndrome or oculosympathetic palsy, comprises ipsilateral ptosis, miosis, and facial anhidrosis. CASE REPORT: We report herein the case of a 67-year-old man who presented with congenital HS associated with ipsilateral hypoplasia o...
Autores principales: | Deprez, Fabrice C., Coulier, Julie, Rommel, Denis, Boschi, Antonella |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neurological Association
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387487/ https://www.ncbi.nlm.nih.gov/pubmed/25749818 http://dx.doi.org/10.3988/jcn.2015.11.2.192 |
Ejemplares similares
-
Artistic Iris: A Case of Congenital Sectoral Heterochromia Iridis
por: Tomar, Mandeep, et al.
Publicado: (2018) -
Post-thyroidectomy iatrogenic Horner's syndrome with heterochromia
por: Ulusoy, Mahmut Oğuz, et al.
Publicado: (2016) -
Congenital agenesis of internal carotid artery with ipsilateral Horner presenting as focal neurological symptoms
por: Farhat, Wassim, et al.
Publicado: (2011) -
A novel mutation of the StAR gene with congenital adrenal hyperplasia and its association with heterochromia iridis: a case report
por: Splittstösser, Vera, et al.
Publicado: (2019) -
A Case of Woolly Hair Nevus Associated with Pigmentary Demarcation Lines and Heterochromia Iridis: Coincidence or a New Association?
por: Kocak, Aslihan Yonca, et al.
Publicado: (2015)