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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1974 Mar;11(1):41–49. doi: 10.1136/jmg.11.1.41

The Trismus-Pseudocampylodactyly Syndrome

B G A Ter Haar *, R F Van Hoof
PMCID: PMC1013087  PMID: 4837286

Abstract

A new family with the combination of trismus and curvature of the fingers on dorsiflexion of the wrist is described. Data from 24 affected members of this family make it likely that the measurements of mouth opening and of wrist angles are sufficient to recognize the syndrome. The affected persons also show a mild degree of short stature but only when compared with their unaffected sibs of the same sex. In the pronounced cases of trismus the coronoid process is enlarged by the extensive pull of the temporal muscle tendon unit which decreases the mandibular excursion. Surgical correction of the enlarged coronoid process may then be necessary.

The variable expressivity of this autosomal dominant trait makes it most likely that the phenotypes in the families described hitherto are due to the same mutation.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Smith R. J., Kaplan E. B. Camptodactyly and simialr atraumatic flexion deformities of the proximal interphalangeal joints of the fingers. A study of thirty-one cases. J Bone Joint Surg Am. 1968 Sep;50(6):1187–1203. [PubMed] [Google Scholar]

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