Thompson E, Pembrey M
J Med Genet. 1985 Jun;22(3):192-201. doi: 10.1136/jmg.22.3.192.
Five children in whom a diagnosis of Seckel syndrome had previously been made were re-examined in the genetic unit. One child had classical Seckel syndrome, a sib pair had the features of the syndrome with less severe short stature, and in two children the diagnosis was not confirmed. Seckel syndrome is only one of a group of low birth weight microcephalic dwarfism and careful attention should be paid to fulfillment of the major criteria defined by Seckel before the diagnosis is made. There remains a heterogeneous group of low birth weight microcephalic dwarfism yet to be defined.
曾被诊断为塞克尔综合征的5名儿童在遗传科接受了重新检查。1名儿童患有典型的塞克尔综合征,1对同胞具有该综合征特征但身材矮小程度较轻,另有2名儿童的诊断未得到证实。塞克尔综合征只是低出生体重小头侏儒症群体中的一种,在做出诊断前应仔细关注塞克尔所定义的主要标准是否满足。仍有一组异质性的低出生体重小头侏儒症有待明确。