نتایج جستجو برای: lhon

تعداد نتایج: 362  

2017

Leber's hereditary optic neuropathy (LHON)-plus is a maternally inherited genetic disorder of young males and characterized by severe progressive vision loss with other neurological and systemic symptoms. Here we present a young male with subacute progressive vision loss and Parkinsonism symptoms like right arm rigidity and endocrine abnormalities like hypoparathyroidism as a probable LHON-plus...

2012
Alessandro Achilli Luisa Iommarini Anna Olivieri Maria Pala Baharak Hooshiar Kashani Pascal Reynier Chiara La Morgia Maria Lucia Valentino Rocco Liguori Fabio Pizza Piero Barboni Federico Sadun Anna Maria De Negri Massimo Zeviani Helene Dollfus Antoine Moulignier Ghislaine Ducos Christophe Orssaud Dominique Bonneau Vincent Procaccio Beate Leo-Kottler Sascha Fauser Bernd Wissinger Patrizia Amati-Bonneau Antonio Torroni Valerio Carelli

BACKGROUND Leber's hereditary optic neuropathy (LHON) is a maternally inherited blinding disorder, which in over 90% of cases is due to one of three primary mitochondrial DNA (mtDNA) point mutations (m.11778G>A, m.3460G>A and m.14484T>C, respectively in MT-ND4, MT-ND1 and MT-ND6 genes). However, the spectrum of mtDNA mutations causing the remaining 10% of cases is only partially and often poorl...

2015
Ayako Mizoguchi Yuki Hashimoto Yasuhiro Shinmei Mayo Nozaki Kan Ishijima Yoshiaki Tagawa Susumu Ishida

BACKGROUND Leber's hereditary optic neuropathy (LHON) refers to an optic nerve dysfunction due to mutations in the mitochondrial DNA, resulting in visual loss by apoptosis of retinal ganglion cells (RGC). In 20% of LHON cases, their fundus examination looks entirely normal at early stage. There are some reports regarding the circumpapillary retinal nerve fiber layer (cpRNFL) and the ganglion ce...

Journal: :Archives of neurology 2007
Liesbeth Spruijt Hubert J Smeets Alexandra Hendrickx Marijke Wefers Bettink-Remeijer A Maat-Kievit Kees C Schoonderwoerd Wim Sluiter Ireneaus F de Coo Rogier Q Hintzen

OBJECTIVE To report a novel mutation that is associated with Leber hereditary optic neuropathy (LHON) within the same family affected by spastic dystonia. DESIGN Leber hereditary optic neuropathy is a mitochondrial disorder characterized by isolated central visual loss. Of patients with LHON, 95% carry a mutation in 1 of 3 mitochondrial DNA-encoded complex I genes. The complete mitochondrial ...

2007
Valerio Carelli Flavia Franceschini Silvia Venturi Piero Barboni Giacomo Savini Giuseppe Barbieri Ettore Pirro Chiara La Morgia Maria L. Valentino Francesca Zanardi Francesco S. Violante Stefano Mattioli

CONTEXT Leber hereditary optic neuropathy (LHON) is a maternally inherited loss of central vision related to pathogenic mutations in the mitochondrial genome, which are a necessary but not sufficient condition to develop the disease. Investigation of precipitating environmental/occupational (and additional genetic) factors could be relevant for prevention. CASE PRESENTATION After a 6-month pe...

2011
Marcela Scabello Amaral-Fernandes Ana Maria Marcondes Paulo Maurício do Amor Divino Miranda Andréa Trevas Maciel-Guerra Edi Lúcia Sartorato

PURPOSE There are many similarities in the clinical presentation of Leber hereditary optic neuropathy (LHON) and in patients who have optic neuropathy and a history of heavy tobacco and alcohol consumption. The main objective of this study is to investigate the frequency of primary and secondary mitochondrial DNA (mtDNA) mutations for LHON in patients diagnosed as having alcohol and tobacco opt...

2013
Nahid Akhtar Khan Periyasamy Govindaraj Vuskamalla Jyothi Angamuthu K Meena Kumarasamy Thangaraj

BACKGROUND Mitochondrial DNA (mtDNA) mutations are known to cause Leber hereditary optic neuropathy (LHON). However, the co-occurrence of double pathogenic mutations with different pathological significance in pedigrees is a rare event. METHODS Detailed clinical investigation and complete mtDNA sequencing analysis was performed for two Indian families with LHON. The haplogroup was constructed...

2014
Raed Behbehani Motasem Melhem Ghazi Alghanim Kazem Behbehani Osama Alsmadi

BACKGROUND Leber's hereditary optic neuropathy (LHON) is a condition characterised by a rapid bilateral central vision loss due to death of the retinal ganglion cells, leading to visual impairment commonly occurring during young adulthood. The disease manifests itself more in male patients than female patients. The mtDNA mutations m.11778G>A, m.3460G>A and m.14484T>C are by far more frequent in...

2010
Manoj Kumar Mukesh Tanwar Rohit Saxena Pradeep Sharma Rima Dada

PURPOSE To screen mitochondrial DNA (mtDNA) variations in Leber hereditary optic neuropathy (LHON). METHODS Ten LHON patients were selected from neuro-ophthalmology clinics of All India Institute of Medical Sciences (AIIMS), New Delhi, India. Clinical evaluation included slit-lamp biomicroscopy, fundus examination, and neuroimaging. DNA was isolated from whole blood samples. The entire coding...

2017
Sandipan Datta Christophe Baudouin Francoise Brignole-Baudouin Alexandre Denoyer Gino A. Cortopassi

Purpose Benzalkonium chloride (BAK) is the most commonly used eye drop preservative. Benzalkonium chloride has been associated with toxic effects such as "dry eye" and trabecular meshwork degeneration, but the underlying biochemical mechanism of ocular toxicity by BAK is unclear. In this study, we propose a mechanistic basis for BAK's adverse effects. Method Mitochondrial O2 consumption rates...

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