Abstract
This paper describes two cases of acrocephalosyndactylia (Apert's syndrome). Both very clearly showed the characteristic malformations. In addition, both patients showed synostosis between the calcaneus and the cuboid bone; this synostosis is not a typical feature of Apert's syndrome, but has been described in the literature once before.
摘要
本文描述了两例尖头并指畸形（阿佩尔氏综合征）。两者均非常清晰地显示出特征性畸形。此外，两名患者均显示跟骨与骰骨之间有骨性融合；这种骨性融合并非阿佩尔氏综合征的典型特征，但此前文献中曾有过描述。
相似文献
1
Apert's syndrome.阿佩尔综合征
Radiol Clin (Basel). 1978;47(4):233-8.
2
The pathogenesis of premature craniosynostosis in acrocephalosyndactyly (Apert's syndrome). A reconsideration.尖头并指（趾）畸形（阿佩尔氏综合征）中颅缝早闭的发病机制。重新审视。
Plast Reconstr Surg. 1977 May;59(5):699-707. doi: 10.1097/00006534-197705000-00013.
3
Radiological case of the month: Apert's syndrome.本月放射病例：阿佩尔综合征。
Am J Dis Child. 1968 Apr;115(4):469-70. doi: 10.1001/archpedi.1968.02100010471010.
4
Apert's acrocephalosyndactyly in mother and daughter: cleft palate in the mother.母女患阿佩尔综合征（尖头并指畸形）：母亲患有腭裂。
Birth Defects Orig Artic Ser. 1971 Jun;7(7):262-4.
5
[Apert's syndrome (acrocephalosyndactylia) in a 6-year-old girl].[一名6岁女童的Apert综合征（尖头并指畸形）]
Pediatr Pol. 1974 Apr;49(4):473-7.
6
Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the lambdoid suture.克鲁宗综合征和阿佩尔综合征中的慢性扁桃体疝：人字缝过早融合的作用
J Neurosurg. 1995 Oct;83(4):575-82. doi: 10.3171/jns.1995.83.4.0575.
7
["Apert's foot" (in acrocephalo-syndactyly) (author's transl)].["阿佩尔氏足"（见于尖头并指（趾）畸形）（作者译）]
Z Orthop Ihre Grenzgeb. 1978 Feb;116(1):1-6.
8
[The ear in Crouzon's and Apert's craniofacial abnormalities].[克鲁宗综合征和阿佩尔综合征颅面畸形中的耳部问题]
Z Laryngol Rhinol Otol. 1971 Nov;50(11):794-802.
9
[Apert's syndrome: the clinico-radiographic picture].[阿佩尔综合征：临床影像学表现]
Arch Putti Chir Organi Mov. 1990;38(1):207-14.
10
[Apert's syndrome in a 4-year-old child].[一名4岁儿童的Apert综合征]
Pediatr Pol. 1974 Apr;49(4):479-82.
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