Literature DB >> 7282770

The King syndrome: malignant hyperthermia, myopathy, and multiple anomalies.

E W McPherson, C A Taylor.   

Abstract

Heterogeneity in malignant hyperthermia is being recognized with increasing frequency. In 1973, King described a subgroup of malignant hyperthermia patients with slowly progressive myopathy, short stature, kyphoscoliosis, pectus carinatum, cryptorchidism, and a characteristic facial appearance. Seven cases have been reported, all in males. We present the case of a girl with similar clinical findings who died in a malignant hyperthermia crisis and review the previously reported cases of King syndrome. The delineation of King syndrome provides further evidence for the heterogeneity of malignant hyperthermia and increases awareness of this disorder; its recognition in a female may lead to preoperative diagnosis and prevention of malignant hyperthermia crisis in King syndrome patients.

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Year:  1981        PMID: 7282770     DOI: 10.1002/ajmg.1320080206

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

Review 1.  To fire the train: a second malignant-hyperthermia gene.

Authors:  K Hogan
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

2.  A recessive form of congenital contractures and torticollis associated with malignant hyperthermia.

Authors:  U G Froster-Iskenius; J R Waterson; J G Hall
Journal:  J Med Genet       Date:  1988-02       Impact factor: 6.318

3.  Typical and atypical presentation of malignant hyperpyrexia in nonwhite patients.

Authors:  W C Parris; J Kambam; B Adkins
Journal:  Anesth Prog       Date:  1988 Sep-Oct
  3 in total

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