Coenzyme Q10 Therapy in Hereditary Motor Sensory Neuropathy Type VI with Novel Mitofusin 2 Mutation
スポンサーリンク
概要
- 論文の詳細を見る
Hereditary motor sensory neuropathy type VI (HMSN VI) is hereditary neuropathy accompanied by optic neuropathy. The feasibility of Coenzyme Q10 (CoQ10) as a treatment for subacute visual impairment of HMSN VI was examined.A 37-year-old patient with HMSN VI with a novel mitofusin 2 mutation was treated with high dose of CoQ10 (200 mg/day) for eight months.Visual impairment was partially resolved after CoQ10 therapy.High dose CoQ10 therapy may improve the prognosis of subacute visual impairment in HMSN VI. To confirm the effectiveness of CoQ10 on HMSN VI, further studies are needed.
著者
-
Takahashi Ryoichi
Department Of Agriculture Government Research Institute
-
Yamada Masahito
Department Of Neurology & Neurobiology Of Aging Kanazawa University Graduate School Of Medical S
-
Iwasa Kazuo
Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Japan
-
Takahashi Ryoichi
Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Japan
-
Ikeda Tokuhei
Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Japan
-
Hamaguchi Ayumi
Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Japan
関連論文
- Multiple cranial nerve enhancement on MRI in primary Sjテカgren's syndrome
- Familial ALS with G298S Mutation in TARDBP: A Comparison of CSF Tau Protein Levels with those in Sporadic ALS
- CD20- and CD56-Positive T-Cell Large Granular Lymphocyte Leukemia in a Human T-Cell Leukemia Virus Type 1 Carrier
- Polyethylene Glycol Interferon α-2b-induced Immune-mediated Polyradiculoneuropathy
- Modified and Fuzzified General Problem Solver for "Monkey and Banana" Problem : Strategy of General Problem Solver
- Reduced expression of endogenous secretory receptor for advanced glycation endproducts in hippocampal neurons of Alzheimer’s disease brains
- Geographic Difference of Mortality of Creutzfeldt-Jakob Disease in Japan
- Peripheral and multiple cranial neuropathies in a 74-year-old woman
- Aging of the human limbic system: Observations of centenarian brains and analyses of genetic risk factors for senile changes
- Dementia of the Alzheimer type and related dementias in the aged: DAT subgroups and senile dementia of the neurofibrillary tangle type
- Embolic Stroke with a Patent Foramen Ovale and Behcet's Disease
- Significance of ^I-MIBG scintigraphy as a pathophysiological indicator in the assessment of Parkinson's disease and related disorders : It can be a specific marker for Lewy body disease
- Multiple Skull Metastases from Hepatocellular Carcinoma Successfully Treated with Radiotherapy
- Fisher Syndrome Associated with Immune Thrombocytopenic Purpura
- Amyotrophic lateral sclerosis : frequent complications by cervical spondylosis
- Autopsy case of sporadic Creutzfeldt-Jakob disease presenting with signs suggestive of brainstem and spinal cord involvement
- Cerebral amyloid angiopathy : An overview
- Senile dementia of the neurofibrillary tangle type (tangle-only dementia) : Neuropathological criteria and clinical guidelines for diagnosis
- MRI of adult-onset type II citrullinemia
- Plasmacytoma of the Urinary Bladder in a Renal Transplant Recipient
- The first Japanese patient with variant Creutzfeldt-Jakob disease (vCJD)
- The risk of iatrogenic Creutzfeldt-Jakob disease through medical and surgical procedures
- Dura mater graft-associated Creutzfeldt-Jakob disease in Japan : Clinicopathological and molecular characterization of the two distinct subtypes
- Alternative BSE Risk Assessment Methodology of Imported Beef and Beef Offal to Japan
- Duration of Prion Disease is Longer in Japan Than in Other Countries
- NOTES ON APHIDS FOUND NEAR THE SUMMIT OF MT. NIITAKA, FORMOSA (HOMOPTERA)
- Effects of intravenous immunoglobulin therapy in Japanese patients with polymyositis and dermatomyositis resistant to corticosteroids : a randomized double-blind placebo-controlled trial
- Coenzyme Q10 Therapy in Hereditary Motor Sensory Neuropathy Type VI with Novel Mitofusin 2 Mutation
- Immunoglobulin light-chain (AL) amyloidosis with myasthenic symptoms and echocardiographic features of dilated cardiomyopathy
- A linear lesion along the brachial plexus on FDG-PET in neurolymphomatosis
- The Response to Second-line Induction with Bortezomib and Dexamethasone is Predictive of Long-term Outcomes Prior to High-dose Chemotherapy with Autologous Stem Cell Transplantation for Multiple Myeloma
- The Chemical Behavior of Low Valence Sulfur Compounds. IV. The Solubility of Ammonium Thiosulfate in Aqueous Ammonia
- NOTES ON THE ALEYRODIDAE OF JAPAN (HOMOPTERA), I
- Model-Based Temperature Noise Monitoring Methods for LMFBR Core Anomaly Detection.