[家族性婴儿皮质增生症（作者译）]
[Familial infantile cortical hyperostosis (author's transl)].
作者信息
Baldellou Vázquez A, Gomá Brufau A, Carreras Calvete A, Used Aznar M D, Gómez Beltrán J L
出版信息
An Esp Pediatr. 1979 Feb;12(2):155-8.
PMID:371475
Abstract
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.
摘要
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。
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