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Gemignani, Franco; Percesepe, Antonio; Gualandi, Francesca; Allegri, Isabella; Bellanova, Maria Federica; Nuredini, Andi; Saccani, Elena; Ambrosini, Enrico; Barili, Valeria; Uliana, Vera
International journal of molecular sciences, 02/2024, Letnik: 25, Številka: 3Journal Article
Charcot-Marie-Tooth disease (CMT) rarely presents with painful symptoms, which mainly occur in association with myelin protein zero ( ) gene mutations. We aimed to further characterize the features of painful neuropathic phenotypes in -related CMT. We report on a 58-year-old woman with a longstanding history of intermittent migrant pain and dysesthesias. Examination showed minimal clinical signs of neuropathy along with mild changes upon electroneurographic examination, consistent with an intermediate pattern, and small-fiber loss upon skin biopsy. Genetic testing identified the heterozygous variant p.Trp101Ter in . We identified another 20 CMT patients in the literature who presented with neuropathic pain as a main feature in association with mutations, mostly in the extracellular domain; the majority of these patients showed late onset (14/20), with motor-nerve-conduction velocities predominantly in the intermediate range (12/20). It is hypothesized that some mutations could manifest with, or predispose to, neuropathic pain. However, the mechanisms linking mutations and pain-generating nerve changes are unclear, as are the possible role of modifier factors. This peculiar CMT presentation may be diagnostically misleading, as it is suggestive of an acquired pain syndrome rather than of an inherited neuropathy.
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