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Postaxial limb hypoplasia (PALH): the classification, clinical features, and related developmental biology
Zeng Zhang1, Dan Yi2, Rong Xie2
1Department of Orthopedic Surgery, Shanghai Jiao-Tong University Affiliated Sixth People's Hospital, Shanghai, China.
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.
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