ALLMedicine™ Optic Atrophy Center
Research & Reviews 1,341 results
https://doi.org/10.1016/j.bbr.2021.113187
Behavioural Brain Research; Gaines CH, Snyder AE et. al.
Feb 21st, 2021 - Wolfram syndrome (WFS) is a rare autosomal recessive disorder characterized by diabetes mellitus and insipidus, progressive optic atrophy and sensorineural deafness. An increased incidence of psychiatric disorders has also been reported in WFS pat...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868283
BMJ Case Reports; Reddy S, Tyagi M et. al.
Feb 5th, 2021 - A 69-year-old male patient presented to the retina clinic with a sudden decrease in vision in his right eye since 1 day. He was a known case of granulomatosis with polyangiitis and was on systemic immunosuppression for the past 3 years. The best-c...
https://doi.org/10.1007/s10792-021-01711-6 10.1212/WNL.0000000000000200 10.1097/WCO.0b013e328341f94a 10.1016/j.ncl.2014.01.001 10.1007/s00415-017-8401-7 10.3109/02688697.2010.544783 10.1038/eye.1998.18 10.1016/j.sjopt.2014.09.016 10.1016/j.ophtha.2015.06.003 10.1007/s00415-011-6273-9 10.1007/s00417-010-1465-z 10.1167/iovs.08-2528 10.1007/s13760-018-1000-2 10.1007/s00415-010-5750-x 10.1212/WNL.0000000000002774 10.1038/eye.2010.139 10.1038/eye.2011.277 10.1016/j.ophtha.2009.05.025 10.1167/tvst.4.5.7 10.1177/1756285616635987 10.1093/brain/114.2.1112 10.1001/archopht.1982.01030030137016 10.1016/S0161-6420(95)30883-4 10.1167/iovs.14-14960 10.1007/978-1-4613-8525-7 10.1016/j.ophtha.2017.04.035 10.1016/j.clineuro.2011.05.015
International Ophthalmology; Kabatas N, Eren Y et. al.
Jan 22nd, 2021 - To use optic coherence tomography (OCT) to evaluate idiopathic intracranial hypertension (IIH) patients with subclinical segmental optic atrophy despite being under apparently effective treatment. IIH patients underwent an OCT examination includin...
https://doi.org/10.1007/s11011-021-00671-1 10.1136/jmedgenet-2012-101146 10.1007/s00439-015-1568-z 10.1002/1531-8249(200009)48:3<330::AID-ANA7>3.0.CO;2-A 10.1038/ng1095-144 10.1093/hmg/ddx273 10.1002/ajmg.a.37986 10.1038/ng.378 10.1136/jmedgenet-2013-101932 10.3389/fonc.2019.00053 10.1038/ejhg.2010.83 10.1038/ejhg.2014.80 10.1038/gim.2015.30 10.1016/j.mito.2010.03.001 10.1007/s11064-019-02786-5 10.1016/j.cell.2005.05.025 10.1002/ana.410390212 10.1210/jc.2017-01762 10.1136/jmg.2007.054270
Metabolic Brain Disease; Zehavi Y, Saada A et. al.
Jan 20th, 2021 - Isolated defects in the mitochondrial respiratory chain complex II (CII; succinate-ubiquinone oxidoreductase) are extremely rare and mainly result from bi-allelic mutations in one of the nuclear encoded subunits: SDHA, SDHB and SDHD, which compris...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809849
BMC Neurology; Bazvand F, Keramatipour M et. al.
Jan 16th, 2021 - To report a novel mutation and new clinical findings in a case with SPOAN syndrome (spastic paraplegia, optic atrophy, neuropathy). Clinical examination, genetic testing and electroretinography were used to study a 2-year-old child who was referre...
Clinicaltrials.gov 1,349 results
https://doi.org/10.1016/j.bbr.2021.113187
Behavioural Brain Research; Gaines CH, Snyder AE et. al.
Feb 21st, 2021 - Wolfram syndrome (WFS) is a rare autosomal recessive disorder characterized by diabetes mellitus and insipidus, progressive optic atrophy and sensorineural deafness. An increased incidence of psychiatric disorders has also been reported in WFS pat...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868283
BMJ Case Reports; Reddy S, Tyagi M et. al.
Feb 5th, 2021 - A 69-year-old male patient presented to the retina clinic with a sudden decrease in vision in his right eye since 1 day. He was a known case of granulomatosis with polyangiitis and was on systemic immunosuppression for the past 3 years. The best-c...
https://doi.org/10.1007/s10792-021-01711-6 10.1212/WNL.0000000000000200 10.1097/WCO.0b013e328341f94a 10.1016/j.ncl.2014.01.001 10.1007/s00415-017-8401-7 10.3109/02688697.2010.544783 10.1038/eye.1998.18 10.1016/j.sjopt.2014.09.016 10.1016/j.ophtha.2015.06.003 10.1007/s00415-011-6273-9 10.1007/s00417-010-1465-z 10.1167/iovs.08-2528 10.1007/s13760-018-1000-2 10.1007/s00415-010-5750-x 10.1212/WNL.0000000000002774 10.1038/eye.2010.139 10.1038/eye.2011.277 10.1016/j.ophtha.2009.05.025 10.1167/tvst.4.5.7 10.1177/1756285616635987 10.1093/brain/114.2.1112 10.1001/archopht.1982.01030030137016 10.1016/S0161-6420(95)30883-4 10.1167/iovs.14-14960 10.1007/978-1-4613-8525-7 10.1016/j.ophtha.2017.04.035 10.1016/j.clineuro.2011.05.015
International Ophthalmology; Kabatas N, Eren Y et. al.
Jan 22nd, 2021 - To use optic coherence tomography (OCT) to evaluate idiopathic intracranial hypertension (IIH) patients with subclinical segmental optic atrophy despite being under apparently effective treatment. IIH patients underwent an OCT examination includin...
https://doi.org/10.1007/s11011-021-00671-1 10.1136/jmedgenet-2012-101146 10.1007/s00439-015-1568-z 10.1002/1531-8249(200009)48:3<330::AID-ANA7>3.0.CO;2-A 10.1038/ng1095-144 10.1093/hmg/ddx273 10.1002/ajmg.a.37986 10.1038/ng.378 10.1136/jmedgenet-2013-101932 10.3389/fonc.2019.00053 10.1038/ejhg.2010.83 10.1038/ejhg.2014.80 10.1038/gim.2015.30 10.1016/j.mito.2010.03.001 10.1007/s11064-019-02786-5 10.1016/j.cell.2005.05.025 10.1002/ana.410390212 10.1210/jc.2017-01762 10.1136/jmg.2007.054270
Metabolic Brain Disease; Zehavi Y, Saada A et. al.
Jan 20th, 2021 - Isolated defects in the mitochondrial respiratory chain complex II (CII; succinate-ubiquinone oxidoreductase) are extremely rare and mainly result from bi-allelic mutations in one of the nuclear encoded subunits: SDHA, SDHB and SDHD, which compris...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809849
BMC Neurology; Bazvand F, Keramatipour M et. al.
Jan 16th, 2021 - To report a novel mutation and new clinical findings in a case with SPOAN syndrome (spastic paraplegia, optic atrophy, neuropathy). Clinical examination, genetic testing and electroretinography were used to study a 2-year-old child who was referre...
News 2 results
https://reference.medscape.com/viewarticle/884107_6
Sep 24th, 2019 - Question 1 of 2 Which of the following conditions is not associated with congenital LQTS? Your Peers Chose: Congenital sensorineural hearing loss 0% Congenital optic atrophy 0% Syncopal attacks 0% Seizures 0% Sudden cardiac death 0% Important clue...
https://www.medscape.com/viewarticle/732033_4
Nov 9th, 2010 - Discussion There are 2 forms of this disease. The classic form usually begins in childhood and manifests with dysarthria, rigidity, spasticity, dystonia, hyperreflexia, Babinski signs, and deterioration of cognitive faculties. Optic atrophy and se...
