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Dominantly inherited malignant hyperthermia (MH) in the King–Denborough Syndrome

✍ Scribed by Dr. Hyam Isaacs; Margaret E. Badenhorst


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
770 KB
Volume
15
Category
Article
ISSN
0148-639X

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✦ Synopsis


Abstract

A 14‐year‐old boy, an only child, with the phenotypical dysmorphic features of the King–Denborough Syndrome developed a severe hyperthermic episode during anesthesia which responded to the administration of sodium dantrolene. As adequate metabolic studies were not available at the time of the crisis he was referred for confirmation of the malignant hyperthermia (MH) status. Muscle tension studies confirmed the presence of MH. The patient's mother and father were subsequently tested and the mother was found to be MH positive, the father MH negative.