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Page 1
Clinical and imaging clues to the diagnosis and follow-up of ptosis and ophthalmoparesis.
Keene KR, Kan HE, van der Meeren S, Verbist BM, Tannemaat MR, Beenakker JM, Verschuuren JJGM. Keene KR, et al. J Cachexia Sarcopenia Muscle. 2022 Dec;13(6):2820-2834. doi: 10.1002/jcsm.13089. Epub 2022 Sep 29. J Cachexia Sarcopenia Muscle. 2022. PMID: 36172973 Free PMC article. Review.
Ophthalmoparesis and ptosis can be caused by a wide range of rare or more prevalent diseases, several of which can be successfully treated. ...Each pattern was linked to anatomical locations and either hereditary or acquired diseases. Hereditary muscle diseases often lead …
Ophthalmoparesis and ptosis can be caused by a wide range of rare or more prevalent diseases, several of which can be successfully tr …
Clinical Characteristics and Treatment Response of Chronic Inflammatory Demyelinating Polyradiculoneuropathy.
Suanprasert N, Hanchaiphiboolkul S. Suanprasert N, et al. J Med Assoc Thai. 2017 Mar;100(3):262-9. J Med Assoc Thai. 2017. PMID: 29911781
Autonomic symptoms, respiratory failure, bulbar involvement, ophthalmoparesis, ptosis, and muscle atrophy were rarely presented. The treatment response was generally favorable. ...
Autonomic symptoms, respiratory failure, bulbar involvement, ophthalmoparesis, ptosis, and muscle atrophy were rarely presented. The …
Progressive External Ophthalmoplegia in Polish Patients-From Clinical Evaluation to Genetic Confirmation.
Kierdaszuk B, Kaliszewska M, Rusecka J, Kosińska J, Bartnik E, Tońska K, Kamińska AM, Kostera-Pruszczyk A. Kierdaszuk B, et al. Genes (Basel). 2020 Dec 31;12(1):54. doi: 10.3390/genes12010054. Genes (Basel). 2020. PMID: 33396418 Free PMC article.
Twenty-six patients had mitochondrial encephalomyopathy (ME), six patients Kearns-Sayre syndrome (KSS), and one patient sensory ataxic neuropathy, dysarthria, ophthalmoparesis (SANDO) syndrome. Genetic analysis of nDNA genes revealed the presence of pathogenic or possibly …
Twenty-six patients had mitochondrial encephalomyopathy (ME), six patients Kearns-Sayre syndrome (KSS), and one patient sensory ataxic neuro …
Guillain-Barre Syndrome, variants & forms fruste: Reclassification with new criteria.
Hiew FL, Ramlan R, Viswanathan S, Puvanarajah S. Hiew FL, et al. Clin Neurol Neurosurg. 2017 Jul;158:114-118. doi: 10.1016/j.clineuro.2017.05.006. Epub 2017 May 4. Clin Neurol Neurosurg. 2017. PMID: 28514704
RESULTS: All patients initially identified as GBS or related disorders can be sub-classified into having classical GBS (41, 67%), classic Miller-Fisher Syndrome (MFS) (6, 10%), Pharyngeal-cervical-brachial (PCB) (3, 5%), paraparetic GBS (4, 7%), bifacial weakness with paresthesia …
RESULTS: All patients initially identified as GBS or related disorders can be sub-classified into having classical GBS (41, 67%), classic Mi …
Mild clinical manifestation and unusual recovery upon coenzyme Q10 treatment in the first Chinese Leigh syndrome pedigree with mutation m.10197 G>A.
Chen Z, Zhao Z, Ye Q, Chen Y, Pan X, Sun B, Huang H, Zheng A. Chen Z, et al. Mol Med Rep. 2015 Mar;11(3):1956-62. doi: 10.3892/mmr.2014.2911. Epub 2014 Nov 10. Mol Med Rep. 2015. PMID: 25384404
The Leigh syndrome (LS), characterized by psychomotor retardation, seizures, nystagmus, ophthalmoparesis, optic atrophy, ataxia, dystonia, or respiratory failure, is one of the most severe mitochondrial diseases. ...
The Leigh syndrome (LS), characterized by psychomotor retardation, seizures, nystagmus, ophthalmoparesis, optic atrophy, ataxia, dyst …
Mitochondrial DNA (mtDNA) diseases: correlation of genotype to phenotype.
Morgan-Hughes JA, Sweeney MG, Cooper JM, Hammans SR, Brockington M, Schapira AH, Harding AE, Clark JB. Morgan-Hughes JA, et al. Biochim Biophys Acta. 1995 May 24;1271(1):135-40. doi: 10.1016/0925-4439(95)00020-5. Biochim Biophys Acta. 1995. PMID: 7599199 Free article.
Even within the MELAS subgroup, the majority of patients had one or more clinical manifestations considered to be atypical of the MELAS syndrome. They included developmental delay, ophthalmoparesis, pigmentary retinopathy and intestinal pseudo-obstruction. ...
Even within the MELAS subgroup, the majority of patients had one or more clinical manifestations considered to be atypical of the MELAS synd …
Evaluation of bupivacaine-induced muscle regeneration in the treatment of ptosis in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome.
Andrews RM, Griffiths PG, Chinnery PF, Turnbull DM. Andrews RM, et al. Eye (Lond). 1999 Dec;13 ( Pt 6):769-72. doi: 10.1038/eye.1999.225. Eye (Lond). 1999. PMID: 10707142
Whilst surgical shortening of the levator muscle can mechanically elevate the lid, this procedure does not restore normal movement and leaves patients at risk of corneal exposure due to concomitant ophthalmoparesis. Recent studies have shown that bupivacaine-induced muscle …
Whilst surgical shortening of the levator muscle can mechanically elevate the lid, this procedure does not restore normal movement and leave …