نتایج جستجو برای: بیماری lhon

تعداد نتایج: 44681  

Journal: :Brain : a journal of neurology 2014
Michio Hirano

Among mitochondrial diseases, Leber hereditary optic neuropathy (LHON) stands out as a prototype in several respects. It was the first mitochondrial disease to be clinically recognized by Dr Albrecht von Graefe (1858) but was named after Dr Theodore Leber who, 13 years after the original report, described 15 patients with the disease, from four different families (Leber, 1871). LHON also has th...

2015
Siobhan Eustace Ryan Fergus Ryan David Barton Veronica O’Dwyer Derek Neylan

BACKGROUND Leber's Hereditary Optic Neuropathy (LHON; MIM 535000) is one of the most commonly inherited optic neuropathies and it results in significant visual morbidity among young adults with a peak age of onset between the ages of 15-30. The worldwide incidence of LHON is approximately 1 in 31,000. 95 % of LHON patients will have one of 3 primary mitochondrial mutations, G3460A (A52T of ND1)...

Journal: :Investigative ophthalmology & visual science 2017
Rustum Karanjia Adriana Berezovsky Paula Yuri Sacai Nivea Nunes Cavascan Henry Yuheng Liu Samir Nazarali Milton Nunes Moraes-Filho Kirsten Anderson Jeffrey Show Tran Sung EunSong Watanabe Milton Nunes Moraes Federico Sadun Anna Maria DeNegri Piero Barboni Carolina do Val Ferreira Ramos Chiara La Morgia Valerio Carelli Rubens Belfort Stuart Glenn Coupland Solange Rios Salomao Alfredo A Sadun

Purpose The photopic negative response (PhNR) is a slow negative component of a flash photopic full-field ERG that has been shown to be specific for retinal ganglion cell (RGC) activity. Direct evaluation of RGC function is desirable in patients with Leber's hereditary optic neuropathy (LHON) in which the loss of central acuity can make it difficult to monitor patients with standard metrics. Th...

Journal: :Investigative ophthalmology & visual science 2017
Angelica Bianco Vittoria Petruzzella

We appreciate the interest of Prof. J. Finsterer in our recent publication entitled ‘‘High Mitochondrial DNA Copy Number Is a Protective Factor From Vision Loss in Heteroplasmic Leber’s Hereditary Optic Neuropathy (LHON)’’ published in IOVS. We would like to clarify some points that required comments. Mutations in the mitochondrial (mt)DNA associated with LHON are generally homoplasmic and pene...

Journal: :Molecular genetics and metabolism 2011
Gary Fruhman Megan L Landsverk Timothy E Lotze Jill V Hunter Michael F Wangler Adekunle M Adesina Lee-Jun C Wong Fernando Scaglia

Leber hereditary optic neuropathy (LHON) is caused by point mutations in mitochondrial DNA (mtDNA), and is characterized by bilateral, painless sub-acute visual loss that develops during the second decade of life. Here we report the case of a five year old girl who presented with clinical and neuroradiological findings reminiscent of Leigh syndrome but carried a mtDNA mutation m.11778G>A (p.R34...

2017
Raymond C.B. Wong Shiang Y. Lim Sandy S.C. Hung Stacey Jackson Shahnaz Khan Nicole J. Van Bergen Elisabeth De Smit Helena H. Liang Lisa S Kearns Linda Clarke David A. Mackey Alex W. Hewitt Ian A. Trounce Alice Pébay

Cybrid technology was used to replace Leber hereditary optic neuropathy (LHON) causing mitochondrial DNA (mtDNA) mutations from patient-specific fibroblasts with wildtype mtDNA, and mutation-free induced pluripotent stem cells (iPSCs) were generated subsequently. Retinal ganglion cell (RGC) differentiation demonstrates increased cell death in LHON-RGCs and can be rescued in cybrid corrected RGCs.

2012
Kazuhiro Nakaso Yoshiki Adachi Emi Fusayasu Koji Doi Keiko Imamura Kenichi Yasui Kenji Nakashima

BACKGROUND Leber's hereditary optic neuropathy (LHON) is a mitochondrial disorder with optic nerve atrophy. Although there are no other associated neurological abnormalities in most cases of LHON, cases of "LHON plus" have been reported. CASE REPORT The proband was a 37-year-old man who had visual and gait disturbances that had first appeared at 10 years of age. He showed horizontal gaze pals...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1997
H Cock R Mandler W Ahmed A H Schapira

Devic's neuromyelitis optica is a rare syndrome characterised by the combination of acute or subacute optic neuritis and transverse myelitis, in some cases considered to be a variant of multiple sclerosis. Mutations of mitochondrial DNA (mtDNA) associated with Leber hereditary optic neuropathy (LHON) have been identified in some patients with multiple sclerosis in whom optic neuritis is a promi...

2016
Ruijin Ran Shuo Yang Heng He Shiqi Ma Zhiqi Chen Bin Li

The objective of this study is to investigate the characteristics and the evolution of visual field damage caused by Leber's hereditary optic neuropathy (LHON) and to provide clinical data for the diagnosis of LHON. Parameters of visual field in 32 consecutive patients (49 eyes) with LHON who were confirmed by genetic diagnostic tests were retrospectively measured within 1 week, between three t...

Journal: :Investigative ophthalmology & visual science 2003
Xiaoping Qi Alfred S Lewin William W Hauswirth John Guy

PURPOSE Reactive oxygen species (ROS) are suspected to play a pivotal role in the pathogenesis of Leber hereditary optic neuropathy (LHON), caused by mutated complex I subunit genes. It seems surprising that optic neuropathy has not been described in animals with a knockout of genes encoding critical anti-ROS defenses. If ROS have a role in the optic nerve injury of LHON, then increasing mitoch...

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