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Infantile Cortical Hyperostosis: Case Report

✍ Scribed by DE OLIVEIRA, THAÍS FEITOSA LEITÃO; DA SILVA SAMPIERI, MARCELO BONIFÁCIO; YAEDU, RENATO YASSUTAKA FARIA; FERREIRA, OSNY; RUBIRA-BULLEN, IZABEL REGINA FISCHER; SARMENTO, VIVIANE ALMEIDA; DA SILVA SANTOS, PAULO SÉRGIO

Book ID
122330140
Publisher
Elsevier
Year
2014
Tongue
English
Weight
54 KB
Volume
117
Category
Article
ISSN
2212-4403

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Familial infantile cortical hyperostosis
Familial infantile cortical hyperostosis
✍ L. Emmery; J. Timmermans; J. Christens; J. P. Fryns 📂 Article 📅 1983 🏛 Springer 🌐 English ⚖ 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.