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Roussy-Lévy syndrome: a case of genotype–phenotype correlation

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References

  1. Roussy G, Levy G (1926) Sept cas d’une maladie familiale particuliere: troubles de la marche, pieds bots et areflexie tendineuse generalisee, avec, accessoirement, legere maladresse des mains. Rev Neurol(Paris) 1:427–450

    Google Scholar 

  2. Planté-Bordeneuve V, Guiochon-Mantel A, Lacroix C, Lapresle J, Said G (1999) The Roussy-Lévy family: from the original description to the gene. Ann Neurol 46(5):770–773. https://doi.org/10.1002/1531-8249(199911)46:5<770

    Article  PubMed  Google Scholar 

  3. Online Mendelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM Number: 159440: 11/27/2018: . World Wide Web URL: https://omim.org/entry/159440. Accessed 21 June 2021

  4. Magy L, Mathis S, Le Masson G, Goizet C, Tazir M, Vallat JM (2018) Updating the classification of inherited neuropathies: results of an international survey. Neurology 90(10):e870–e876. https://doi.org/10.1212/WNL.0000000000005074

    Article  PubMed  Google Scholar 

  5. Kochański A, Drac H, Jedrzejowska H, Hausmanowa-Petrusewicz I (2003) Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short report. Eur J Neurol 10(5):547–549. https://doi.org/10.1046/j.1468-1331.2003.00640.x

    Article  PubMed  Google Scholar 

  6. Warner LE, Hilz MJ, Appel SH, Killian JM, Kolodry EH, Karpati G, Carpenter S, Watters GV, Wheeler C, Witt D, Bodell A, Nelis E, Van Broeckhoven C, Lupski JR (1996) Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination. Neuron 17(3):451–460. https://doi.org/10.1016/s0896-6273(00)80177-4

    Article  CAS  PubMed  Google Scholar 

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Correspondence to Ettore Cioffi.

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This study has been approved by our appropriate ethics committee (Comitato Etico Lazio 2) and has been performed in accordance with the ethical standards laid down in the Declaration of Helsinki. We received written informed consent by the patient.

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The corresponding author declares no competing interests.

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Cioffi, E., Gioiosa, V., Serrao, M. et al. Roussy-Lévy syndrome: a case of genotype–phenotype correlation. Neurol Sci 42, 4357–4358 (2021). https://doi.org/10.1007/s10072-021-05451-4

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