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A Rare Case in the Emergency Department: Holmes-Adie Syndrome [PDF]

open access: hybridTurkish Journal of Emergency Medicine, 2015
SUMMARY: Holmes-Adie syndrome (HAS) is a rare syndrome characterized by tonic pupil and the absence of deep tendon reflexes. HAS was first described in 1931 and is usually idiopathic, with incidences reported to be 4-7 per 100,000.
Sahin COLAK   +6 more
doaj   +3 more sources

Adie-Holmes syndrome associated with COVID-19 infection: A case report

open access: diamondIndian Journal of Ophthalmology, 2021
With increasing experience, it has been suggested that the SARS-CoV-2 virus has a neurotropic effect. Here, we present a case of a tonic pupil who developed after COVID-19 infection.
Nurhan Kaya Tutar   +2 more
doaj   +3 more sources

Adie-Holmes Syndrome [PDF]

open access: diamondRevista Brasileira de Oftalmologia, 2015
The Holmes-Adie syndrome is characterized by the presence of tonic pupil associated with absence or diminution of deep tendon reflexes. In some cases there may be autonomous nerve dysfunction.
Renato Antunes Schiave Germano   +6 more
doaj   +3 more sources

Holmes-Adie syndrome. [PDF]

open access: bronzeJ Neurol Neurosurg Psychiatry, 1980
3–5 The tonic pupil of patients with this syndrome is initially monolateral, but frequently progresses to involve the other eye. Onset is usually gradual and is often noticed by an observer rather than by the patient. On slit lamp examination the pupillary sphincter muscle shows spontaneous movements in some segments that appear worm-like—so-called ...
Martinelli P, Montagna P, Gabellini AS.
europepmc   +5 more sources

A hypothetical immunemediated unifying mechanism for the Holmes-Adie syndrome [PDF]

open access: hybridArquivos de Neuro-Psiquiatria, 1988
The Holmes-Adie syndrome consists of pupillotonia, arreflexia and autonomic dysfunction. Some explanations for these different symptoms have been attempted, centred upen neuropathological and electrophysiological findings.
C. M. de Castro Costa   +2 more
doaj   +2 more sources

Ross syndrome following COVID-19 infection in an 18-year-old Syrian male patient: a case report [PDF]

open access: yesJournal of Medical Case Reports
Background Ross syndrome is an exceptionally rare disorder characterized by tonic pupils, areflexia, and anhidrosis, with a prevalence that appears to be higher in women than in men, typically presenting in individuals during their 30s.
Ahed Assaf   +5 more
doaj   +2 more sources

ADIE SYNDROME AS A COMPLICATION OF CHICKENPOX

open access: diamondДетские инфекции (Москва), 2018
Adie syndrome is a rare complication of chickenpox, which is seen in female mainly up to 6 years of age, one week after vesicular rash appearance.Aim: to introduce a case report of Adie syndrome as a complication of chickenpox.Material and methods: a ...
I. T. Todorov   +2 more
doaj   +3 more sources

Adie’s pupil and systemic manifestations: a rare unilateral presentation [PDF]

open access: yesGMS Ophthalmology Cases
We present a case of a young woman who presented with blurring of vision in her right eye, worsening on near work. Detailed ophthalmic and neurological evaluation was done, which revealed light near dissociation, vermiform iris movements, constriction to
Vimisha, M N   +3 more
doaj   +2 more sources

Management of Adie Syndrome

open access: bronzeOptometry and Vision Science, 1981
In most instances the patient with pupillotonia presents with under accommodation in the affected eye. An unusual case of Adie's pupil with ciliary spasm is discussed. As a result of the unpredictable accommodative response, the necessity of evaluating and prescribing for binocular balance is underscored.
K, Horkovičová   +2 more
  +8 more sources

Abnormal pupils at the bedside: rapid recognition of neurologic and systemic emergencies in acute care settings [PDF]

open access: yesInternational Journal of Emergency Medicine
Background Pupillary abnormalities are critical bedside findings that may indicate both benign physiologic variation and life-threatening neurologic emergencies.
Dawn C. Penney   +2 more
doaj   +2 more sources

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