Acute Orbital Apex Syndrome Caused by Idiopathic Sclerosing Orbital Inflammation
Diagnostics, 2022 Idiopathic sclerosing orbital inflammation (ISOI) is a distinct entity among other orbital diseases. It is characterized by marked fibrosis and inflammatory cell infiltration that can damage orbital structures.
Chung-Chih Chang +7 more
doaj +1 more source
Dominant BIN1-related centronuclear myopathy (CNM) revealed by lower limb myalgia and moderate CK elevation [PDF]
, 2015 We report a BIN1-related CNM family with unusual clinical phenotype. The proband, a 56-year-old man suffered of lower limbs myalgia since the age of 52.
Antonini, Giovanni +8 more
core +1 more source
Clinical insights on Tolosa Hunt syndrome: a multidisciplinary approach on neurological-related symptomatology in maxillofacial region [PDF]
, 2018 Background Tolosa–Hunt syndrome (THS) related neurological symptoms are described in literature as “unilateral”, “recurrent”, “episodic”, “intense”, “severe”, “lancinating” or “stabbing” pain on the upper face and forehead and may be misdiagnosed ...
Ahmed Siddiqui, Ammar +8 more
core +2 more sources
The importance of social history in the work-up of painful ophthalmoplegia
Interdisciplinary Neurosurgery, 2014 Painful ophthalmoplegia is not one uncommon clinic phenomenon in both ophthalmological and neurological clinics, which can be caused by various pathological conditions and easily be misdiagnosed by some clinical practitioners.
Jun Mu, MD, PhD +2 more
doaj +1 more source
Clinical efficacy of the partial rectus muscle transportation procedure for paralytic strabismus [PDF]
International Journal of Ophthalmology, 2020 AIM: To analyze the clinical efficacy of the partial rectus muscle transportation (PRT) procedure for paralytic strabismus due to single rectus muscle palsy.
Yan-Qiong Tu +3 more
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An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement [PDF]
, 1981 An 81-year-old man from a family with a history of oculopharyngeal muscular dystrophy (OPMD) involving 6 members over 4 generations is described. The patient first noted drooping of his eyelids at the age of 65.
Aarli +49 more
core +1 more source
Recurrent painful ophthalmoplegic neuropathy: a report of two new pediatric cases
The Turkish Journal of Pediatrics, 2022 Background. Recurrent painful ophthalmologic neuropathy (RPON), formerly known as ophthalmoplegic migraine, is characterized by repeated attacks of one or more ocular cranial nerve palsies with an ipsilateral headache.
Çağatay Günay +4 more
doaj +1 more source
Seeing double: the low-carb diet [PDF]
, 2013 No abstract ...
Drummond, Russell S. +4 more
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Progression of myopathology in Kearns-Sayre syndrome [PDF]
, 1992 We report on the progression of myopathology by comparing two biopsies from a patient with a Kearns-Sayre-Syndrome. The first biopsy was taken in 1979 and showed 10% ragged-red fibers.
B. Meurers +11 more
core +1 more source
Alexandria Journal of Medicine, 2014 Introduction: Lesions in medial longitudinal fasciculus (MLF) produce internuclear ophthalmoplegia (INO) with characteristic horizontal gaze abnormality.
Yeshigeta Gelaw
doaj +1 more source