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Partial lipodystrophy presenting with myopathy

Published online by Cambridge University Press:  01 February 1999

S J Moore
Affiliation:
Department of Medical Genetics, Aberdeen Royal Hospitals Trust, Aberdeen, UK.
I A Auchterlonie
Affiliation:
Department of Paediatrics, Aberdeen Royal Hospitals Trust, Aberdeen, UK.
G F Cole
Affiliation:
Department of Paediatrics, Aberdeen Royal Hospitals Trust, Aberdeen, UK.
E S Gray
Affiliation:
Department of Pathology, Aberdeen Royal Hospitals Trust, Aberdeen, UK.
J C S Dean
Affiliation:
Department of Medical Genetics, Aberdeen Royal Hospitals Trust, Aberdeen, UK.
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Abstract

A girl with partial lipodystrophy is described presenting with muscle weakness and developmental delay several years before lipoatrophy became apparent. The patient subsequently developed epilepsy, fatty liver, secondary amenorrhoea, hirsutism, insulin-resistant diabetes mellitus, hyperlipidaemia, and hypothyroidism. She remains weak with poor exercise tolerance. This case illustrates an atypical presentation of the Barraquer–Simon syndrome.

Type
Case Reports
Copyright
© 1999 Mac Keith Press

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