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Research Article

Hereditary Neuropathy with Liability to Pressure Palsy: A Brief Review with a Case Report

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Pages 119-123 | Received 12 Jul 2011, Published online: 30 Nov 2011

REFERENCES

  • Hui-Chou HG, Hashemi SS, Hoke A, & Dellon AL. Clinical implications of peripheral myelin. J Reconstr Microsurg. 2011;27:67–73.
  • Chance PF. Inherited focal, episodic neuropathies. NeuroMol Med. 2006;8:159–74.
  • Li J, Krajewski K, Shy ME, & Lewis RA. Hereditary neuropathy with liability to pressure palsy. Neurology. 2002;58:1769–73.
  • Taioli F, Cabrini I, Cavallaro T, Acler M, & Fabrizi GM. Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene. Brain. 2011;134: 608–17.
  • Dubourg O, Mouton P, Brice A, LeGuern E, & Bouche P. Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsy. Neuromuscul Disord. 2000;10:206–8.
  • Koc F, Guzel R, Benliday IC, Yerdelen D, Güzel I, & Sarca Y. A rare genetic disorder in the differential diagnosis of the entrapment in neuropathies: hereditary neuropathy with pressure palsies. J Rheumatol. 2006;12:78–82.
  • Li J, Krajewski K, Shy ME, Lewis RA. Hereditary neuropathy with liability to pressure palsy. Neurology. 2002;58:1769–73.
  • Behse F, Butchal F, Carlsen F, Hereditary neuropathy with liability to pressure palsies: electrophysiological and histopathological aspects. Brain. 1972;95:777–94.
  • Sessa M, Nemni R, Quattrini A, Del Carro U, Wrabetz L, & Canal L. Atypical hereditary neuropathy with liability to pressure palsies (HNPP): the value of direct DNA diagnosis. J Med Genet. 1997;34:889–2.
  • Chance P, Alderson M, Leppig K, Lensch MW, Matsunami N, Smith B, Swanson PD, Odelberg SJ, Disteche CM, & Bird TD. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell. 1993;15:143–51.
  • Snipes G, Suter U, Welcher A, & Shooter EM. Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13). J Cell Biol. 1992;117:225–38.
  • Meuleman J, Pou-Serradell A, Löfgren A, Ceuterick C, Martin JJ, Timmerman V, Van Broeckhoven C, & De Jonghe P. A novel 3′-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies. Neuromuscul Disord. 2001;11:400–3.
  • Pareyson D, Taroni F. Deletion of the PMP22 gene and hereditary neuropathy with liability to pressure palsies. Curr Opin Neurol. 1996;9:348–54.
  • Tsairis P, Dyck P, Mulder D. Natural history of brachial plexus neuropathy. Report on 99 patients. Arch Neurol. 1972;27:109–17.
  • Ørstavik K, Heier MS, Young P, & Stögbauer F. Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies. Muscle Nerve. 2001;24:1093–6.
  • Taggart T, Allan T. Surgical treatment of a tomaculous neuropathy. J R Coll Surg Edinb. 2001;46:240–1.

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