Baldellou Vázquez A, Gomá Brufau A, Carreras Calvete A, Used Aznar M D, Gómez Beltrán J L
An Esp Pediatr. 1979 Feb;12(2):155-8.
A new case of familial Caffey's disease is referred with focused clinic, radiologic and anatopathologic aspects. The hereditary patterns may obey a autosomic dominant one, with variable penetrance and expressivity. Thus a improved familial research is necessary in all the infantile cortical hyperostosis cases.
本文报告了1例伴有重点临床、放射学及病理解剖学特征的家族性婴儿骨皮质增生症。遗传模式可能符合常染色体显性遗传，具有可变的外显率和表现度。因此，对于所有婴儿骨皮质增生症病例，均需加强家族性研究。
