{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,23]],"date-time":"2025-10-23T05:20:37Z","timestamp":1761196837171},"reference-count":45,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2007,9,21]],"date-time":"2007-09-21T00:00:00Z","timestamp":1190332800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Inher Metab Disea"],"published-print":{"date-parts":[[2007,10]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>Although they are classically viewed as paediatric diseases, it is now recognized that inborn errors of metabolism (IEMs) can present at any age from childhood to adulthood. IEMs can involve the peripheral nervous system, mostly as part of a more diffuse neurological or systemic clinical picture. However, in some cases, the neuropathy can be the unique initial sign. Here, based on our personal experience and on a comprehensive literature analysis, we review IEMs causing neuropathies in adults. Diseases were classified according to the predominant type of neuropathies into (1) acute neuropathies, (2) mononeuropathy multiplex, (3) chronic axonal polyneuropathies, (4) chronic demyelinating polyneuropathies, (5) small\u2010fibre neuropathies, and (6) lower motor neuron disease.<\/jats:p>","DOI":"10.1007\/s10545-007-0684-x","type":"journal-article","created":{"date-parts":[[2007,9,18]],"date-time":"2007-09-18T23:17:51Z","timestamp":1190157471000},"page":"642-653","source":"Crossref","is-referenced-by-count":36,"title":["Peripheral neuropathy and inborn errors of metabolism in adults"],"prefix":"10.1002","volume":"30","author":[{"given":"F.","family":"Sedel","sequence":"first","affiliation":[{"name":"Federation of Nervous System Diseases, Salp\u00eatri\u00e8re Hospital 47 Boulevard de l'H\u00f4pital Paris cedex 13 75651 France"},{"name":"Federation of Nervous System Diseases, The Salp\u00eatri\u00e8re Hospital Pierre et Marie Curie University Assistance Publique\u2010H\u00f4pitaux de Paris Paris France"},{"name":"Reference Center for Lysosomal Diseases, The Salp\u00eatri\u00e8re Hospital Pierre et Marie Curie University Assistance Publique\u2010H\u00f4pitaux de Paris Paris France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Barnerias","sequence":"additional","affiliation":[{"name":"Department of Pediatry and Metabolic Diseases, Reference Center for Metabolic Diseases, Necker\u2010Enfants Malades Hospital Ren\u00e9\u2010Descartes University Assistance Publique\u2010H\u00f4pitaux de Paris Paris France"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"O.","family":"Dubourg","sequence":"additional","affiliation":[{"name":"Reference Center for Neuromuscular Diseases and Institute of Myology, The Salp\u00eatri\u00e8re Hospital Pierre et Marie Curie University Assistance Publique\u2010H\u00f4pitaux de Paris Paris 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