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외안근마비를 동반한 선천성근섬유형불균형증 1예

A Case of Congenital Fiber Type Disproportion Associated with External Ophthalmoplegia

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초록

Abstract

Congenital fiber type disproportion (CFTD) is a form of congenital myopathy characterized by histologic findings of the smallness of type 1 fiber and type 1 fiber predominance. It is usually associated with hypotonia and motor weakness of the limb muscles at birth or the neonatal period. We report a 6-year-old girl with limb weakness and ophthalmoplegia, whose muscle pathology showed the classic pattern of CFTD without any other abnormality.

참고문헌 (8)

  1. "congenital fiber type disproportion-30 years on", 62, pp.977~989 (2003)
  2. "A girl with 1p36 deletion syndrome and congenital fiber type disproportion myopathy", 47, pp.556~559 (2002)
  3. "Early predictors of poor outcome in congenital fiber-type disproportion myopathy", 49, pp.855~856 (1992)
  4. "Type 1 fiber size disproportion:morphometric data from 37 children with myopathic,neuropathic,or idiopathic hypotonia", 7, pp.395~419 (1987)
  5. "Muscle fiber type disproportion with an autosomal dominant inheritance", 41, pp.281~284 (2000)
  6. "Congenital fiber type disproportion-A pathology in search of a disease Muscle disorders in childhood", pp.166~167 (1995)
  7. "Clinical variability in congenital fiber type disproportion", 46, pp.257~266 (1980)
  8. "Congenital fibre type disproportion myopathy.A histological diagnosis with an uncertain clinical outlook", 54, pp.735~743 (1979)

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