Horton W A, Harris D J, Collins D L
Am J Med Genet. 1983 May;15(1):97-101. doi: 10.1002/ajmg.1320150113.
We describe monozygotic twins with thanatophoric dysplasia who were discordant for the Kleeblattschädel anomaly, but were identical in all other respects, including the histologic appearance of the endochondral growth plate. The observation suggests that the skull anomaly represents a variable manifestation of thanatophoric dysplasia, and that its occurrence in an infant with this bone dysplasia should not alter the low recurrence risk generally given.
我们描述了患有致死性骨发育不全的单卵双胞胎,他们在“风车颅”畸形方面表现不一致,但在所有其他方面都相同,包括软骨内生长板的组织学外观。该观察结果表明,颅骨异常代表了致死性骨发育不全的一种可变表现,并且在患有这种骨发育异常的婴儿中出现这种情况不应改变通常给出的低复发风险。