Literature DB >> 10830040

Antemortem diagnosis of Leigh's disease: role of magnetic resonance studies.

D Ghosh1, S Pradhan.   

Abstract

A two-and-a-half-year-old male child presented with recurrent attacks of intractable vomiting, psychomotor retardation since 14 months of age. He had also lower cranial nerve palsy and corticospinal involvement. Magnetic resonance imaging had shown multiple well circumscribed areas of hypointusity in T1 weighted image which were brightly hyperintense in heavily T2-weighted image. The lesions were seen in basal ganglia, thalamii and brainstem and spared mamillary bodies. Magnetic resonance spectroscopy demonstrated lactate peak in the affected areas confirming the diagnosis of Leigh's disease. The child responded well to large dose of vitamin 'B' therapy.

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Year:  1996        PMID: 10830040     DOI: 10.1007/bf02730822

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  18 in total

1.  Cytochrome c oxidase deficiency and long-chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy.

Authors:  H Reichmann; H Scheel; B Bier; U P Ketelsen; S Zabransky
Journal:  Ann Neurol       Date:  1992-01       Impact factor: 10.422

2.  Subacute necrotizing encephalomyelopathy in an infant.

Authors:  D LEIGH
Journal:  J Neurol Neurosurg Psychiatry       Date:  1951-08       Impact factor: 10.154

3.  Cytochrome c oxidase deficiency in Leigh syndrome.

Authors:  S DiMauro; S Servidei; M Zeviani; M DiRocco; D C DeVivo; S DiDonato; G Uziel; K Berry; G Hoganson; S D Johnsen
Journal:  Ann Neurol       Date:  1987-10       Impact factor: 10.422

4.  Leigh disease (subacute necrotizing encephalomyelopathy): CT and MR in five cases.

Authors:  C A Geyer; K J Sartor; A J Prensky; C L Abramson; F J Hodges; M H Gado
Journal:  J Comput Assist Tomogr       Date:  1988 Jan-Feb       Impact factor: 1.826

5.  Subacute necrotizing encephalomyelopathy (Leigh's disease): a consideration of clinical features and etiology.

Authors:  J H Pincus
Journal:  Dev Med Child Neurol       Date:  1972-02       Impact factor: 5.449

6.  Hyper-endorphin syndrome in a child with necrotizing encephalomyelopathy.

Authors:  N J Brandt; L Terenius; B B Jacobsen; L Klinken; A Nordius; S Brandt; K Blegvad; M Yssing
Journal:  N Engl J Med       Date:  1980-10-16       Impact factor: 91.245

7.  Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high.

Authors:  Y Tatuch; J Christodoulou; A Feigenbaum; J T Clarke; J Wherret; C Smith; N Rudd; R Petrova-Benedict; B H Robinson
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

8.  CT scan appearances in Leigh's disease (subacute necrotizing encephalomyelopathy).

Authors:  K Hall; D Gardner-Medwin
Journal:  Neuroradiology       Date:  1978       Impact factor: 2.804

9.  Subacute necrotizing encephalomyelopathy (Leigh's disease).

Authors:  D W McCandless; W E Hodgkin
Journal:  Pediatrics       Date:  1977-12       Impact factor: 7.124

10.  CT scan appearance in subacute necrotising encephalomyelopathy.

Authors:  J Campistol; E Fernandez Alvarez; V Cusi
Journal:  Dev Med Child Neurol       Date:  1984-08       Impact factor: 5.449

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  3 in total

1.  Leigh's syndrome.

Authors:  A A S R Mannan; M C Sharma; P Shrivastava; A M Ralte; V Gupta; M Behari; C Sarkar
Journal:  Indian J Pediatr       Date:  2004-11       Impact factor: 1.967

2.  Profile of inborn errors of metabolism in a tertiary care centre PICU.

Authors:  Mahesh Kamate; Vivek Chetal; Vijaylaxmi Kulgod; Vishwanath Patil; Rita Christopher
Journal:  Indian J Pediatr       Date:  2010-02-05       Impact factor: 1.967

3.  A rare mitochondrial disorder: Leigh syndrome--a case report.

Authors:  Dhananjay Y Shrikhande; Piyush Kalakoti; M M Aarif Syed; Kunal Ahya; Gurmeet Singh
Journal:  Ital J Pediatr       Date:  2010-09-15       Impact factor: 2.638

  3 in total

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