Literature DB >> 8429443

Diagnosis of occult muscular dystrophy: importance of the "chance" finding of elevated serum aminotransferase activities.

R P Morse1, N P Rosman.   

Abstract

We report our experience with four children, including one girl, in whom the eventual diagnosis of muscular dystrophy was made because of persistent, unexplained elevated serum aminotransferase values. Measurement of serum creatine kinase activity and careful physical examination are the most useful and cost-effective means of correctly identifying these patients.

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Year:  1993        PMID: 8429443     DOI: 10.1016/s0022-3476(06)80126-5

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  3 in total

1.  Isolated elevated serum transaminases leading to the diagnosis of asymptomatic Pompe disease.

Authors:  Marieke Hoeksma; Maartje Boon; Klary E Niezen-Koning; Lidy van Overbeek-van Gils; Francjan J van Spronsen
Journal:  Eur J Pediatr       Date:  2006-10-17       Impact factor: 3.183

2.  Serum Enzyme Profiles Differentiate Five Types of Muscular Dystrophy.

Authors:  Yuling Zhu; Huili Zhang; Yiming Sun; Yaqin Li; Langhui Deng; Xingxuan Wen; Huaqiao Wang; Cheng Zhang
Journal:  Dis Markers       Date:  2015-04-29       Impact factor: 3.434

3.  Anaesthetic management of two patients with pompe disease for caesarean section.

Authors:  I J J Dons-Sinke; M Dirckx; G P Scoones
Journal:  Case Rep Anesthesiol       Date:  2014-03-20
  3 in total

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