Literature DB >> 2398945

Magnetic resonance imaging in MELAS syndrome.

L Rosen1, S Phillips, D Enzmann.   

Abstract

MELAS syndrome is a distinct clinical entity belonging to a group of mitochondrial encephalomyopathies characterized by the tetrad of myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Computed tomography (CT) and magnetic resonance (MR) findings are reviewed in a patient with MELAS. Serial CT studies demonstrated multiple "migrating" infarcts in various stages of evolution involving primarily the posterior temporal and occipital regions. MR was more sensitive than CT in demonstrating the number and extent of cortical lesions in this disease entity.

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Year:  1990        PMID: 2398945     DOI: 10.1007/bf00588572

Source DB:  PubMed          Journal:  Neuroradiology        ISSN: 0028-3940            Impact factor:   2.804


  14 in total

1.  Retinitis pigmentosa, external ophthalmophegia, and complete heart block: unusual syndrome with histologic study in one of two cases.

Authors:  T P KEARNS; G P SAYRE
Journal:  AMA Arch Ophthalmol       Date:  1958-08

2.  Mitochondrial encephalomyopathies: a group of neuromuscular disorders with defects in oxidative metabolism.

Authors:  Y Shapira; S Harel; A Russell
Journal:  Isr J Med Sci       Date:  1977-02

3.  Computed tomography and angiography in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes); report of 3 cases.

Authors:  K Hasuo; S Tamura; K Yasumori; A Uchino; S Goda; S Ishimoto; K Kamikaseda; Y Wakuta; M Kishi; K Masuda
Journal:  Neuroradiology       Date:  1987       Impact factor: 2.804

4.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.

Authors:  S G Pavlakis; P C Phillips; S DiMauro; D C De Vivo; L P Rowland
Journal:  Ann Neurol       Date:  1984-10       Impact factor: 10.422

5.  Mitochondrial encephalopathy, lactic acidosis, and strokelike syndrome (MELAS)

Authors:  M Kuriyama; A Igata
Journal:  Ann Neurol       Date:  1985-11       Impact factor: 10.422

6.  Mitochondrial myopathy. Biochemical studies revealing a deficiency of NADH--cytochrome b reductase activity.

Authors:  J M Land; J A Morgan-Hughes; J B Clark
Journal:  J Neurol Sci       Date:  1981-04       Impact factor: 3.181

7.  Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis.

Authors:  Y Kobayashi; S Miyabayashi; G Takada; K Narisawa; K Tada; T Y Yamamoto
Journal:  Eur J Pediatr       Date:  1982-09       Impact factor: 3.183

8.  Mitochondrial encephalomyopathy with decreased succinate-cytochrome c reductase activity.

Authors:  J E Riggs; S S Schochet; A V Fakadej; A Papadimitriou; S DiMauro; T W Crosby; L Gutmann; R T Moxley
Journal:  Neurology       Date:  1984-01       Impact factor: 9.910

9.  Mitochondrial encephalomyopathy: fluctuating symptoms and CT.

Authors:  T Yamamoto; H Beppu; T Tsubaki
Journal:  Neurology       Date:  1984-11       Impact factor: 9.910

10.  Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature.

Authors:  N Fukuhara; S Tokiguchi; K Shirakawa; T Tsubaki
Journal:  J Neurol Sci       Date:  1980-07       Impact factor: 3.181

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  9 in total

Review 1.  Magnetic resonance imaging in lactic acidosis.

Authors:  M S van der Knaap; C Jakobs; J Valk
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

2.  Clinical, morphological, biochemical, and neuroradiological features of mitochondrial encephalomyopathies. Presentation of 19 patients.

Authors:  A Lindner; E Hofmann; M Naumann; G Becker; H Reichmann
Journal:  Mol Cell Biochem       Date:  1997-09       Impact factor: 3.396

3.  Two unusual clinical presentations of the mitochondrial DNA A3243G point mutation in adult neurological practice.

Authors:  M G Hanna; J R Vaughan; P A Silburn; P T Davis; R C Greenhall; M V Squier; K R Mills; S Renowden; A Sellar
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-05       Impact factor: 10.154

4.  Reversible cortical oedema mimicking cortical dysplasia in mitochondrial disorder.

Authors:  I Tuxhorn; H Holthausen; A Ebner; S Noachtar
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-11       Impact factor: 10.154

5.  The appearance of ADCs in the non-affected areas of the patients with MELAS.

Authors:  Zhenghua Liu; Xiwei Liu; Lihong Hui; Danhua Zhao; Xiaoying Wang; Sheng Xie; Jiangxi Xiao; Xuexiang Jiang
Journal:  Neuroradiology       Date:  2010-06-17       Impact factor: 2.804

6.  Neuroradiological features of six kindreds with MELAS tRNA(Leu) A2343G point mutation: implications for pathogenesis.

Authors:  C M Sue; D S Crimmins; Y S Soo; R Pamphlett; C M Presgrave; N Kotsimbos; M J Jean-Francois; E Byrne; J G Morris
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-08       Impact factor: 10.154

7.  MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity.

Authors:  M G Hanna; I P Nelson; J A Morgan-Hughes; N W Wood
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-10       Impact factor: 10.154

8.  Migratory stroke-like lesions in a case of adult-onset mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome and a review of imaging findings.

Authors:  Stephen S Cai; Rainer von Coelln; Theresa J Kouo
Journal:  Radiol Case Rep       Date:  2016-10-05

9.  Adult-onset mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome with progressive sensorineural hearing loss: A case report.

Authors:  T M Trang; P C Chien; B T Dung; N T H Thu; N T T Truc; V N C Khang
Journal:  Radiol Case Rep       Date:  2021-05-24
  9 in total

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