Literature DB >> 3996454

Multicore disease and Marfan's syndrome: a case report.

M Pagès, B Echenne, A M Pagès, A Dimeglio, A Sires.   

Abstract

A 16-year-old girl with a generalized nonprogressive motor weakness and clinical signs of Marfan's syndrome is reported. A minicore disease was diagnosed after muscle biopsy. The association of Marfan's syndrome with muscular dystrophies is discussed.

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Year:  1985        PMID： 3996454     DOI： 10.1159/000115842

Source DB:  PubMed          Journal:  Eur Neurol        ISSN： 0014-3022            Impact factor:   1.710


  3 in total

1.  Muscle fibrillin deficiency in Marfan's syndrome myopathy.

Authors:  W M H Behan; C Longman; R K H Petty; P Comeglio; A H Child; M Boxer; P Foskett; D G F Harriman
Journal:  J Neurol Neurosurg Psychiatry       Date:  2003-05       Impact factor: 10.154

2.  Dural ectasia is a common feature of the Marfan syndrome.

Authors:  R E Pyeritz; E K Fishman; B A Bernhardt; S S Siegelman
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

3.  Pleocore disease. Multi-minicore disease and focal loss of cross striations.

Authors:  J J Martin; M Bruyland; H F Busch; J P Farriaux; I Krivosic; C Ceuterick
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088
  3 in total

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