Partington M W, Gonzales-Crussi F, Khakee S G, Wollin D G
Arch Dis Child. 1971 Oct;46(249):656-64. doi: 10.1136/adc.46.249.656.
Four cases of the cloverleaf skull syndrome are reported, 3 from Britain and 1 from Canada in a family of German/Irish descent. All cases had generalized chondrodysplastic changes and died at or just after birth. It is suggested that a cloverleaf skull is a previously unrecognized feature of thanatophoric dwarfism. Two affected girls from the same sibship are reported for the first time, suggesting an autosomal recessive type of inheritance. A review of the published material indicates that there may be three distinct syndromes in patients with the cloverleaf skull deformity. (1) The cloverleaf skull is associated with thanatophoric dwarfism and death in the perinatal period. (2) There are localized bony lesions of the skeleton outside the skull. (3) The skeleton outside the skull is normal. In the last two syndromes death may occur at birth, but survival into later childhood is the rule.
本文报告了4例三叶草颅骨综合征病例,其中3例来自英国,1例来自加拿大,患儿家族有德国/爱尔兰血统。所有病例均有全身性软骨发育异常改变,并在出生时或出生后不久死亡。有人提出,三叶草颅骨是致死性侏儒症一种以前未被认识的特征。首次报告了来自同一同胞关系的两名患病女孩,提示为常染色体隐性遗传类型。对已发表资料的回顾表明,三叶草颅骨畸形患者可能存在三种不同的综合征。(1)三叶草颅骨与致死性侏儒症相关,并在围产期死亡。(2)颅骨外骨骼有局限性骨病变。(3)颅骨外骨骼正常。在后两种综合征中,可能在出生时死亡,但通常能存活到儿童后期。