Abstract

The hereditary peripheral neuropathies are a clinically and genetically heterogeneous group of diseases of the peripheral nervous system. Foot deformities, including the common pes cavus, but also hammer toes and twisting of the ankle, are frequently present in patients with hereditary peripheral neuropathy, and often represent one of the first signs of the disease. Pes cavus in hereditary peripheral neuropathies is caused by imbalance between the intrinsic muscles of the foot and the muscles of the leg. Accurate clinical evaluation in patients with pes cavus is necessary to exclude or confirm the presence of peripheral neuropathy. Hereditary peripheral neuropathies should be suspected in those cases with bilateral foot deformities, in the presence of family history for pes cavus and/or gait impairment, and in the presence of neurological symptoms or signs, such as distal muscle hypotrophy of limbs. Herein, we review the hereditary peripheral neuropathies in which pes cavus plays a key role as a “spy sign,” discussing the clinical and molecular features of these disorders to highlight the importance of pes cavus as a helpful clinical sign in these rare diseases.

Highlights

  • Pes cavus is a foot deformity characterized by a high arch of the foot that does not flatten with weight bearing; the deformity can be located in the forefoot, midfoot, hindfoot, or in a combination of all these sites (Figs. 1, 2)

  • We discuss the hereditary peripheral neuropathies (HPN) in which pes cavus plays a key role as a ‘‘spy sign.’’ A clear, complete, and detailed review of clinical and molecular features of these rare disorders may be useful in clinical management and differential diagnosis of patients who present with pes cavus as almost single sign of disease

  • HPN associated with pes cavus Charcot–Marie–Tooth disease The most common form of HPN is hereditary motor and sensory neuropathy (HMSN), called Charcot–Marie– Tooth (CMT) disease

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Summary

REVIEW ARTICLE

S. Piazza • G. Ricci • E. Caldarazzo Ienco • C. Carlesi • L. Volpi • G. Siciliano • M. Mancuso Received: 7 May 2010 / Accepted: 25 September 2010 / Published online: 21 October 2010 Ó The Author(s) 2010. This article is published with open access at Springerlink.com

Introduction
Dominant Recessive
Hereditary neuropathy with liability to pressure palsies
Distal hereditary motor neuropathies
Congenital distal SMA
Etiopathogenesis of pes cavus in HPN
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