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Arthrogryposis multiplex congenita in a monozygotic twin. An intrauterine lesion?

作者信息

Mennen U, Williams E

机构信息

Department of Hand and Microsurgery, Medical University of Southern Africa, South Africa.

出版信息

J Hand Surg Br. 1996 Oct;21(5):647-8. doi: 10.1016/s0266-7681(96)80150-1.

Abstract

Arthrogryposis multiplex congenita is a specific, well-defined congenital deformity which primarily affects muscles of limbs resulting in secondary joint deformities. The aetiology is still uncertain. One of monozygotic twin brothers with classical arthrogryposis multiplex congenita is presented, proving that this specific condition is not genetically transmitted.

摘要

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