Results 21 to 30 of about 5,764 (229)

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

Idiopathic congenital Horner Syndrome. Presentation of a case

open access: yesUkrainian Journal of Ophthalmology, 2023
Horner Syndrome results from an interruption of the sympathetic innervation of the eye. This pathway is a chain of three neurons which originate in the hypothalamus, travels down to spinal cord at the level of lower cervical and upper thoracic levels ...
Leopoldo Garduño-Vieyra   +3 more
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

Backpack Palsy With Horner’s Syndrome [PDF]

open access: yesInternational Journal of Surgery, 2017
Traumatic injuries to the brachial plexus are typically high impact and can be debilitating, life-changing injuries. Backpack palsy is a rare but well-established cause of brachial plexus injury, arising as a result of heavy backpack use. We present an unusual case of backpack palsy with Horner’s syndrome.
Olivia Sharp   +2 more
openaire   +2 more sources

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 57‐Year‐Old Male With Behavioral Variant Frontotemporal Dementia and MATR3 and NOS3 Mutations

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This report presents a case of behavioral variant frontotemporal dementia caused by mutations in the MATR3 and NOS3 genes, aiming to analyze its clinical manifestations and genetic characteristics. For a case presenting with personality changes and gait abnormalities as the initial symptoms, this study conducted a comprehensive analysis of its
Feifei Lin, Saie Huang
wiley   +1 more source

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