Familial infantile cortical hyperostosis
β
L. Emmery; J. Timmermans; J. Christens; J. P. Fryns
π
Article
π
1983
π
Springer
π
English
β 605 KB
Infantile cortical hyperostosis occurred in three generations of a family affecting eight different members. As confirmed in this family, Caffey disease is an autosomal dominant disorder of unknown etiology, with incomplete penetrance and variable expression.