نتایج جستجو برای: ophthalmoplegia

تعداد نتایج: 3418  

Journal: :The British journal of ophthalmology 2008
J Ahn N J Kim H K Choung S W Hwang M Sung M J Lee S I Khwarg

AIMS The aim of the study was to evaluate the results of the frontalis sling operation using silicone rod for the correction of ptosis in chronic progressive external ophthalmoplegia patients. METHODS Chronic progressive external ophthalmoplegia patients who received the frontalis sling operation using silicone rods from 1999 to 2006 were included in this study. The medical records were retro...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1987
M P Carey K Poulton C Hawkins R P Murphy

A case of carnitine palmitoyl transferase deficiency presenting in a 72 year old woman with the clinical picture of ophthalmoplegia plus other muscle weakness is reported. Histological and ultrastructural examination showed the features of a mitochondrial myopathy.

Journal: :Journal of neurology, neurosurgery, and psychiatry 1989
G N Fuller R J Guiloff F Scaravilli J N Harcourt-Webster

Two cases of combined HIV-CMV encephalitis are described. One presented with a sixth nerve palsy and a tetraparesis, the other with an internuclear ophthalmoplegia. Pathologically brain stem involvement was predominantly due to CMV.

Journal: :Indian journal of ophthalmology 1990
G S Rekhi

A case of Kearns - Sayre Syndrome characterized by a triad of external ophthalmoplegia, retinal dystrophy and cardiomyopathy is discussed. Ocular examination and cardiologic screening of family members is requested.

2017
Yi Shiau Ng Helen Powell Nigel Hoggard Doug M. Turnbull Robert W. Taylor Marios Hadjivassiliou

Mitochondrial disease is phenotypically and genetically heterogeneous with an estimated prevalence of 1 in 4,300. Mutations in the POLG gene, encoding the catalytic subunit of DNA polymerase gamma, are an important cause of mitochondrial disease. The spectrum of clinical manifestations in POLG-related mitochondrial disease is variable, with disease onset ranging from adulthood-onset dominant or...

Journal: :Clinical neurology and neurosurgery 1990
Koji Takahashi Makoto Kunishige Masayuki Shinohara Katsuyuki Kubo Hideo Inoue Hiide Yoshino Atsuko Asano Souichi Honda Toshio Matsumoto Takao Mitsui

Epstein-Barr virus (EBV) infection causes a wide range of neurologic and hematologic manifestations. We report a 72-year-old Japanese male patient with severe chronic active EBV infection syndrome (SCAEBV) who presented with Guillain-Barré syndrome (GBS) and developed hemophagocytic lymphohistiocytosis (HLH) several months after the onset of GBS. He showed acute onset of distal muscle weakness,...

Journal: :American journal of ophthalmology 1973
P E Romano W J Stark

The presenting symptoms of ocular myasthenia gravis are blepharoptosis and diplopia. These are the result of myasthénie weakening of the levator palpebrae and the extraocular muscles (external ophthalmoplegia), respectively." Blurring of near vision is a frequently as­ sociated symptom, which is due to a fatigue of accommodation (internal ophthalmoplegia)· Blurring of distant vision in ocular m...

Journal: :Journal of Clinical Case Reports 2016

Journal: :The Journal of Nervous and Mental Disease 1898

Journal: :Delhi Journal of Ophthalmology 2020

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