Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2010 Dec;11(4):195-201.
doi: 10.1007/s10195-010-0114-y. Epub 2010 Oct 21.

Pes cavus and hereditary neuropathies: when a relationship should be suspected

Affiliations
Review

Pes cavus and hereditary neuropathies: when a relationship should be suspected

S Piazza et al. J Orthop Traumatol. 2010 Dec.

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.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Pes cavus and main en griffe in a patient with CMT1A
Fig. 2
Fig. 2
Pes cavus in a patient with CMT1A
Fig. 3
Fig. 3
When pes cavus might reveal HPN: a proposed diagnostic algorithm. NCS nerve conduction studies, HPN hereditary peripheral neuropathies

References

    1. Japas LM. Surgical treatment of pes cavus by tarsal v-osteotomy: preliminary report. J Bone Joint Surg Am. 1968;50:927–944. - PubMed
    1. Brewerton DA, Sandifer PH, Sweetnam DR. Idiopathic pes cavus: an investigation into its aetiology. Br Med J. 1963;14:659–661. doi: 10.1136/bmj.2.5358.659. - DOI - PMC - PubMed
    1. Pareyson D, Marchesi C. Diagnosis, natural history, and management of Charco-Marie-Tooth disease. Lancet Neurol. 2009;8:654–667. doi: 10.1016/S1474-4422(09)70110-3. - DOI - PubMed
    1. Irobi J, Dierick I, Jordanova A, Claeys KG, De Jonghe P, Timmerman V. Unraveling the genetics of distal hereditary motor neuronopathies. Neuromolecular Med. 2006;8:131–146. doi: 10.1385/NMM:8:1-2:131. - DOI - PubMed
    1. Martyn CN, Hughes RAC. Epidemiology of peripheral neuropathy. J Neurol Neurosurg Psychiatry. 1997;62:310–318. doi: 10.1136/jnnp.62.4.310. - DOI - PMC - PubMed

MeSH terms

LinkOut - more resources