Homma W, Rütt A
Z Orthop Ihre Grenzgeb. 1982 Nov-Dec;120(6):774-9. doi: 10.1055/s-2008-1051395.
We report on observations in the progress of Calcinosis Interstitialis Universalis in three generations of one family. Some members could be followed for more than 20 years. Each member of the family was examined and the course of the disease described. Part of the family underwent functional analysis by a specialist in internal medicine. Our conclusion is, that, at least, in this family, the disease is in all probability, a genetically fixed, dominant hereditary disease.
我们报告了一个家族三代人中泛发性间质性钙质沉着症的进展观察情况。部分成员的病程长达20多年。对该家族的每位成员都进行了检查并描述了疾病进程。家族中的部分成员接受了一位内科专家的功能分析。我们的结论是,至少在这个家族中,该病很可能是一种基因固定的显性遗传病。