Schwartz-Jampel syndrome (chondrodystrophic myotonia)

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Abstract

Schwartz-Jampel syndrome is a rare autosomal recessive disorder. Joint contractures, generalised myotonia, skeletal anomalies, and facial dysmorphism are common features; malignant hyperthermia is a potentially lethal complication during anaesthesia.

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APA

Viljoen, D., & Beighton, P. (1992). Schwartz-Jampel syndrome (chondrodystrophic myotonia). Journal of Medical Genetics, 29(1), 58–62. https://doi.org/10.1136/jmg.29.1.58

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