Results 11 to 20 of about 67,286 (306)

Myasthenia Gravis Mimicking Third Cranial Nerve Palsy: a Case Report

open access: yesJournal of Cancer and Allied Specialties, 2021
Background: The most common pituitary adenoma presentation is a visual field defect and inappropriate pituitary hormone secretion. The compression of the optic chiasma causes visual impairment.
Sardar Ali Khan   +4 more
doaj   +1 more source

etiological Pattern o FBlePHaroPtosis among Patients Presenting in teacHing HosPital

open access: yesJournal of Nepal Medical Association, 2006
The purpose of this study was to find out the etiological pattern of blepharoptosis among patients presenting in BPKLCOS, T.U. Teaching Hospital. This was a hospital based descriptive and cross-sectional study conducted from February 2003 to July 2004.
Raba Thapa, P C Karmacharya, B P Nepal
doaj   +1 more source

Suspensory materials for surgery of blepharoptosis: a systematic review of observational studies [PDF]

open access: yes, 2016
Background Frontalis suspension surgery is considered the procedure of choice in cases of blepharoptosis. Among all the materials used in this type of surgery, ophthalmic and plastic surgeons prefer to use autologous Fascia Lata.
Amorelli, Giulia Maria   +7 more
core   +3 more sources

Characteristic and Correlation Between TIME and Complication After Destructive Eye Procedure Patient at Plastic and Reconstruction Division Sanglah Hospital\u27s Eye Clinic Bali-Indonesia [PDF]

open access: yes, 2012
Destructive eye procedure can be carried out by enucleation, evisceration and excenteration. Some efforts have been developed to reduce the complications, but it still occur within several years after the operation.
Sukartini, D. (D)   +2 more
core   +2 more sources

Acquired ptosis associated with oculomotor and contralateral facial nerve synkinesis: the first reported case [PDF]

open access: yes, 2017
Evidence of oculomotor nerve (ON) synkinesis is a common occurrence following both acquired and congenital III nerve palsy. It is generally accepted that aberrant regeneration is the likely aetiology of synkinesis in acquired III nerve palsy, following ...
Conversi, Andrea   +7 more
core   +2 more sources

Ptosis [PDF]

open access: yesJournal of Neurology, Neurosurgery & Psychiatry, 1974
Twenty-five examples of ptosis occuring with an acute stroke are analysed. Thirteen of these patients had hemispheral infarctions in which ptosis could not be explained by third nerve or sympathetic dysfunction. The ptosis in these `cerebral' cases was bilateral, with other factors such as pyramidal tract damage determining the asymmetry of the ptosis.
openaire   +2 more sources

An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement [PDF]

open access: yes, 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

Acute ptosis as a presentation of preseptal cellulitis leading to cerebral abscess in a patient with uncontrolled diabetes [PDF]

open access: yesMalaysian Family Physician, 2021
Acute ptosis due to preseptal cellulitis requires urgent medical attention, as the infection can extend posteriorly into the orbit, leading to significant visual and cerebral complications.
Nor Roziah Razali , Yao Mun Choo
doaj   +1 more source

Application of the liposuction techniques and principles in specific body areas and pathologies [PDF]

open access: yes, 2011
The buttocks have been a symbol of attraction, sexuality and eroticism since ancient times and therefore, they have an important role in defining the posterior body contour.
Blugerman, Guillermo   +9 more
core   +2 more sources

Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta [PDF]

open access: yes, 2019
Osteogenesis imperfecta (OI) is a heritable connective tissue disorder, mainly characterized by bone fragility and low bone mass. Defects in the type I procollagen-encoding genes account for the majority of OI, but increasingly more rare autosomal ...
Elcioglu, Nursel   +8 more
core   +1 more source

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