Cortina H, Vallcanera A, Andres V, Gracia A, Aparici R, Mari A
Pediatr Radiol. 1979 Apr 19;8(2):87-92. doi: 10.1007/BF00973997.
A group of syndromes is presented whose common characteristic is the absence of pubic ossification at birth with very slow posterior mineralization. This is a radiological finding of interest as it has not been described in other entities. In all the cases shown, moreover, a variable degree of delay in bone age is observed. The increase of space between the pubic bones described in these syndromes is fictious, as it really signifies the existence of non-ossified cartilage. Therefore, they must be differentiated from those which deal with real widening of the symphysis of pubis.
现介绍一组综合征，其共同特征是出生时耻骨无骨化且后部矿化非常缓慢。这是一项有趣的放射学发现，因为在其他疾病中尚未有过描述。此外，在所有所示病例中，均观察到不同程度的骨龄延迟。这些综合征中所描述的耻骨之间间隙的增大是虚构的，因为它实际上意味着存在未骨化的软骨。因此，必须将它们与那些涉及耻骨联合真正增宽的疾病区分开来。
