Results 21 to 30 of about 5,752 (241)

Parkinson's Syndrome Secondary to Congenital Absence of the Left Internal Carotid Artery: a Case Report and Review of the Literature [PDF]

open access: yesZhongguo quanke yixue, 2023
Congenital absence of the internal carotid artery (ICA) is a rare congenital developmental anomaly, which is often associated with carotid canal atresia and structural abnormalities of the ICA. It may be asymptomatic, or shows noticeable symptoms such as
SUN Xiaoling, LI Zhijun
doaj   +1 more source

Unusual case of persistent Horner′s syndrome following epidural anaesthesia and caesarean section

open access: yesIndian Journal of Ophthalmology, 2011
This is a rare case of persistent Horner′s syndrome following epidural anesthesia and Caesarean section. A 33-year-old female presented with persistent ptosis and miosis following epidural anesthesia and Caesarian section several months prior.
Shubhra Goel, Cat Nguyen Burkat
doaj   +1 more source

Painful Horner's syndrome

open access: yesEmergency Medicine Journal, 2008
Carotid artery dissection is a significant cause of ischaemic stroke and the second leading cause among young patients. It commonly presents with Horner’s syndrome associated with headache, facial or neck pain. Diagnosis is now …
C, Costopoulos, R S, Patel, C D, Mistry
openaire   +4 more sources

Pediatric Horner syndrome

open access: yesJournal of American Association for Pediatric Ophthalmology and Strabismus, 1998
The purpose of this study was to define the etiologies of Horner syndrome in the pediatric population.A retrospective review was performed of the medical records of all pediatric Horner syndrome patients (< 18 years old) examined by the pediatric ophthalmology services at two large referral centers.Seventy-three pediatric Horner syndrome patients were ...
A R, Jeffery   +3 more
openaire   +2 more sources

Acquired Horner′s syndrome in an infant: A case report

open access: yesMuller Journal of Medical Sciences and Research, 2014
Horner′s syndrome has varied etiology. We report a case of acquired Horner′s syndrome in an infant. A 3-month-old female child was referred for drooping of right eye upper lid on the second postoperative day following neck surgery.
Sumana J Kamath   +2 more
doaj   +1 more source

Pourfour du Petit Syndrome in a Patient with Thyroid Carcinoma

open access: yesCase Reports in Neurology, 2010
The clinical presentation of Pourfour du Petit syndrome (PdPs) is the opposite of Horner syndrome. Although all disorders underlying Horner syndrome may potentially present as PdPs, very few cases of the latter have been described in the literature.
Sergi Martinez-Ramirez   +2 more
doaj   +1 more source

The Development of Horner Syndrome following a Stabbing

open access: yesCase Reports in Medicine, 2014
The features of Horner Syndrome are miosis, ptosis, enophthalmos, and anhidrosis on the same side as the etiologic pathology. Its causes include tumours, aneurysms, neck and chest surgery, and neck and chest trauma.
Muhammet Sayan, Ali Çelik
doaj   +1 more source

Cervical Disc Herniation and Central Horner Syndrome

open access: yesBrazilian Neurosurgery, 2016
Central Horner syndrome is a rare condition, comprising a unique pathophysiological phenomenon. It results from vascular lesions, head or thoracic trauma.
Luis Rocha   +2 more
doaj   +1 more source

Horner syndrome: tribute to Professor Horner on his 190th birthday

open access: yesArquivos de Neuro-Psiquiatria, 2021
This paper reviews some aspects of the life and work of Professor Johann Friedrich Horner, on the occasion of the 190th anniversary of his birthday and 152 years after the publication of "Über eine Form von Ptosis".
Otto Jesus Hernández Fustes   +5 more
doaj   +1 more source

A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
wiley   +1 more source

Home - About - Disclaimer - Privacy