Literature DB >> 3203479

Glycogenosis with amylopectinoid deposits in a 13-year-old girl.

T Tuñón1, O Bengoechea, J Narbona.   

Abstract

We present a clinical study and muscle biopsy of a 13-year-old female who suffered hypertrophic cardiomyopathy, hepatosplenomegaly and myopathy of prolonged evolution. The muscle biopsy showed a glycogenosis with deposits of amylopectin-like material. Differential diagnosis was made with basophilic degeneration of the myocardium, and with "polyglucosan bodies disease." In the existing literature we found only one case of juvenile amylopectinosis, and another four adult cases.

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Year:  1988        PMID: 3203479

Source DB:  PubMed          Journal:  Clin Neuropathol        ISSN: 0722-5091            Impact factor:   1.368


  2 in total

1.  New data on the ultrastructure of the corpus amylaceum (polyglucosan body).

Authors:  L Leel-Ossy
Journal:  Pathol Oncol Res       Date:  2001       Impact factor: 3.201

2.  Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis).

Authors:  J M Schröder; R May; Y S Shin; M Sigmund; S Nase-Hüppmeier
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

  2 in total

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