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muscular dystrophies/demam
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A comparison of the stress and coping strategies between the parents of children with Duchenne muscular dystrophy and children with a fever.
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This university hospital-based case control study included 31 parents with a Duchenne muscular dystrophy (DMD) child and 30 parents (control group) of a child with a fever. The study was conducted in southern Taiwan. The study compared the differences of stress and coping strategies between the two
[Malignant hyperthermia of Duchenne muscular dystrophy: application of clinical grading scale and caffeine contracture of skinned muscle fibers].
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Episodes of acute myoglobinuria or cardiac arrest were occasionally complicated in general anesthesia of patients with Duchenne or Becker muscular dystrophy (DMD/BMD). Whether these complications are malignant hyperthermia (MH) or not has several times been discussed. In the present study, we
[Malignant hyperthermia-like reactions in Duchenne or Becker muscular dystrophy: review and hypothesis].
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Adverse reactions to genral anesthesia, which partly resembled malignant hyperthermia (MH), were more frequent in muscular dystrophy than in controls. In the present study, 35 cases so far reported in Duchenne or Becker muscular dystrophy (DMD or BMD) were analyzed and their pathogenesis was
Duchenne muscular dystrophy and malignant hyperthermia--two case reports.
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The case histories are presented including the anaesthetic and postoperative management, of two children, a two-year-old with undiagnosed Duchenne muscular dystrophy (DMD) and a three-year-old with known DMD. The child with undiagnosed DMD had no symptoms of DMD and had received halothane twice
Malignant hyperthermia in a patient with Becker muscular dystrophy: dystrophin analysis and caffeine contracture study.
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We present a 17-year-old boy with Becker muscular dystrophy (BMD) who developed hyperthermia and heart failure after general anesthesia. He presented clinical features of malignant hyperthermia (MH), and had masseter spasm and elevated body temperature (38.7 degrees C) with very high serum CK
Malignant hyperthermia and muscular dystrophies.
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BACKGROUND
Patients with muscular dystrophy have been reported to experience a variety of life-threatening complications during and after general anesthesia. We performed a systematic analysis to define the spectrum of anesthetic-related complications in patients with muscular dystrophy, with an
Muscular dystrophy and malignant hyperthermia--similiar signs.
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Malignant hyperthermia in Duchenne muscular dystrophy.
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[Amyotrophic lateral sclerosis, myasthenia gravis, Duchenne muscular dystrophy or also a questionable disposition to malignant hyperthermia … : Systematics of anesthesiological management in neuromuscular diseases]
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Dental treatment for a patient with Duchenne muscular dystrophy and malignant hyperthermia.
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Malignant hyperthermia susceptibility in patients with Duchenne's muscular dystrophy.
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Malignant hyperthermia in a child with Duchenne muscular dystrophy.
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Duchenne's muscular dystrophy and malignant hyperthermia: another warning.
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[Clinical implications of enhanced caffeine contracture in malignant hyperthermia (MH) and Duchenne muscular dystrophy (DMD)].
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The caffeine contracture response was studied on the skinned muscle fiber in patients with MH episodes or with DMD. An abnormally enhanced caffeine contracture was observed in 12 out of 14 subjects with MH episodes and 11 out of 13 patients with DMD. The extent of abnormality was almost the same in
Duchenne muscular dystrophy and malignant hyperthermia: a genetic study of the ryanodine receptor in 47 patients.
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