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pubmed-article:3267818pubmed:abstractTextThe marked heterogeneity of nemaline myopathy is again shown in the present series of 13 patients. Most children have a long-standing, mild, and slowly progressing proximal myopathy. Two brothers with extreme weakness died during the neonatal period of respiratory failure representing the X-linked variant. One adult with proximal weakness was also diagnosed as having nemaline myopathy. An unusual course was observed in 2 infants who initially had moderate weakness but subsequently developed severe generalized weakness including respiratory muscles. This led to irreversible respiratory failure requiring continuous ventilatory support for as long as 9 and 15 years, respectively. Although uncommon, the possibility of an imminent respiratory failure in initially weak infants should also be taken into account within the clinical spectrum of nemaline myopathy.lld:pubmed
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pubmed-article:3267818pubmed:authorpubmed-author:ShaharEElld:pubmed
pubmed-article:3267818pubmed:authorpubmed-author:MurphyE GEGlld:pubmed
pubmed-article:3267818pubmed:authorpubmed-author:TervoR CRClld:pubmed
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pubmed-article:3267818pubmed:pagination236-40lld:pubmed
pubmed-article:3267818pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:3267818pubmed:articleTitleHeterogeneity of nemaline myopathy. A follow-up study of 13 cases.lld:pubmed
pubmed-article:3267818pubmed:affiliationChild Neurology Unit, Sheba Medical Center, Tel Hashomer, Israel.lld:pubmed
pubmed-article:3267818pubmed:publicationTypeJournal Articlelld:pubmed
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