J Korean Pediatr Soc.  1982 Jan;25(1):97-101.

A Case of Progressive Muscular Dystrophy

Affiliations
  • 1Dept. of Pediatrics Keimyung University of Medicine Taegu, Korea.
  • 2Dept. of Pathology Keimyung University College of Medicine Taegu, Korea.

Abstract

We want to report one case of Duchenne type muscular dystrophy in a female. This patient was seven years of age. Clinical symptoms first appeared at age 3 and progressed insiduously. The Gower's sign was positive. She had a borther who had similar clinical signs and symptoms. He died at age 12. An increased ratio of creatine and creatinine was noted in the patient, with high titers of S.G.O.T., L.D.H. and C.P.K. The muscle biopsy findings showed typical advanced histological changes, that is, great variations in the size of muscle fibers, interstitial fibrosis and infiltration of fat.

Keyword

Duchenne type; muscular dystrophy; in a female

MeSH Terms

Biopsy
Creatine
Creatinine
Female
Fibrosis
Humans
Muscular Dystrophies*
Creatine
Creatinine
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