Two Cases of Evans Myopathy in a Family
Journal of the Korean Neurological Association
;
: 568-570, 2002.
Article
Dans Coréen
| WPRIM
| ID: wpr-192480
ABSTRACT
Evans myopathy is a type of malignant hyperthermia showing characteristic distribution of myopathic changes. We present two cases of Evans myopathy, father and his son in a family. Five members of this family expired during ane sthesia and surgery and two of these cases were reported as the malignant hyperthermia. The muscle pathology shows moth-eaten appearance with or without unstained cores in NADH-TR stain and its difference between the father and his son is suggestive of rather progressive myopathy than static one. s
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Anatomopathologie
/
Pères
/
Hyperthermie maligne
/
Maladies musculaires
Limites du sujet:
Humains
langue:
Coréen
Texte intégral:
Journal of the Korean Neurological Association
Année:
2002
Type:
Article
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