Literature DB >> 508131

Basal ganglia calcification in Kearns-Sayre syndrome.

W C Robertson, C Viseskul, Y E Lee, R V Lloyd.   

Abstract

The Kearns-Sayre syndrome (KSS) appears to be a distinctive disorder characterized by progressive external ophthalmoplegia, pigmentary degeneration of the retina, heart block, and elevated CSF protein levels. Recent reports have suggested that abnormalities of muscle mitochondria may also be a consistent finding in KSS. We recently examined a patient with KSS whose skeletal muscle contained abnormal mitochondria. In addition, a computerized tomographic scan of the head showed cerebellar and brain stem atrophy, as well as calcification in the region of the basal ganglia.

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Year:  1979        PMID: 508131     DOI: 10.1001/archneur.1979.00500470081017

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  4 in total

1.  Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.

Authors:  C Doriguzzi; L Palmucci; T Mongini; N Bresolin; L Bet; G Comi; R Lala
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-01       Impact factor: 10.154

2.  Computed tomography in mitochondrial cytopathy.

Authors:  J Egger; B E Kendall
Journal:  Neuroradiology       Date:  1981       Impact factor: 2.804

3.  Intrinsic laryngeal muscles in oculocraniosomatic syndrome (OCSS). An autopsy study.

Authors:  H P Schmitt; H G Lenard
Journal:  Arch Otorhinolaryngol       Date:  1983

4.  Kearns-Sayre syndrome. A case of the complete syndrome with encephalic leukodystrophy and calcification of basal ganglia.

Authors:  P Carboni; M Giacanelli; G Porro; G Sideri; A Paolella
Journal:  Ital J Neurol Sci       Date:  1981-08
  4 in total

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