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Infantile cortical hyperostosis andCOL1A1mutation in four generations

✍ Scribed by Paola Cerruti-Mainardi; Giacomo Venturi; Marianna Spunton; Elena Favaron; Michela Zignani; Sandro Provera; Bruno Dallapiccola

Book ID
106122294
Publisher
Springer
Year
2011
Tongue
English
Weight
410 KB
Volume
170
Category
Article
ISSN
0340-6997

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✍ Beth M. Drinkwater; Jude P. Crino; Jose Garcia; James Ogburn; Jacqueline T. Hech 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 61 KB 👁 2 views

Infantile cortical hyperostosis (ICH), Caffey disease, is a multifocal, inflammatory skeletal process with classic onset before the fifth month of life and resolution by the age of 3 years. A severe phenotype with early prenatal onset has also been described. Inheritance is generally accepted as aut