David A, Vincent M, Quéré M-P, Lefrançois T, Frampas E, David A
Department of Radiology and Medical Imaging, Hôtel Dieu, CHU de Nantes, 1, place Alexis-Ricordeau, 44093 Nantes cedex 1, France.
Department of Clinical Genetics, hôpital mère-enfant, CHU de Nantes, 7, quai Moncousu, 44000 Nantes, France.
Diagn Interv Imaging. 2015 May;96(5):443-8. doi: 10.1016/j.diii.2014.12.007. Epub 2015 Mar 7.
Brachydactyly, or shortening of the digits, is due to the abnormal development of phalanges, metacarpals and/or metatarsals. This congenital malformation is common, easily detectable clinically but often requires additional radiological exploration. Radiographs are essential to characterize the type of brachydactyly and to show the location of the bone shortening, as well as any associated malformation. This article reviews the radiological findings for isolated brachydactylies (according to the types classified by Bell, and Temtamy and McKusick) and for brachydactylies that are part of complex multisystem malformation syndromes. If warranted by the clinical and radiological examinations, a genetic analysis (molecular and/or cytogenetic) can confirm the etiologic diagnosis.
短指畸形,即手指缩短,是由于指骨、掌骨和/或跖骨发育异常所致。这种先天性畸形很常见,临床上易于发现,但通常需要进一步的影像学检查。X线片对于明确短指畸形的类型、显示骨骼缩短的部位以及任何相关畸形至关重要。本文回顾了孤立性短指畸形(根据Bell、Temtamy和McKusick分类的类型)以及作为复杂多系统畸形综合征一部分的短指畸形的影像学表现。如果临床和影像学检查有必要,基因分析(分子和/或细胞遗传学)可以确诊病因。