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轴后肢体发育不全(PALH):分类、临床特征及相关发育生物学

Postaxial limb hypoplasia (PALH): the classification, clinical features, and related developmental biology.

作者信息

Zhang Zeng, Yi Dan, Xie Rong, Hamilton John L, Kang Qing-Lin, Chen Di

机构信息

Department of Orthopedic Surgery, Shanghai Jiao-Tong University Affiliated Sixth People's Hospital, Shanghai, China.

Department of Orthopedic Surgery, Rush University Medical Center, Chicago, Illinois.

出版信息

Ann N Y Acad Sci. 2017 Dec;1409(1):67-78. doi: 10.1111/nyas.13440. Epub 2017 Oct 9.

Abstract

Postaxial limb hypoplasia (PALH) is a group of nonhereditary diseases with congenital lower limb deficiency affecting the fibular ray, including fibular hemimelia, proximal femoral focal deficiency, and tarsal coalition. The etiology and the developmental biology of the anomaly are still not fully understood. Here, we review the previous classification systems, present the clinical features, and discuss the developmental biology of PALH.

摘要

轴后肢体发育不全(PALH)是一组非遗传性疾病,伴有影响腓骨侧的先天性下肢缺陷,包括腓骨半肢畸形、股骨近端局灶性缺损和跗骨联合。该异常的病因和发育生物学仍未完全明确。在此,我们回顾既往的分类系统,介绍临床特征,并探讨轴后肢体发育不全的发育生物学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c19a/5730483/a172efe741e2/nihms889627f1.jpg

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