Literature DB >> 23207550

Electrophysiological comparison between males and females in HNPP.

Fiore Manganelli1, Chiara Pisciotta, Raffaele Dubbioso, Valerio Maruotti, Rosa Iodice, Francesca Notturno, Lucia Ruggiero, Carmine Vitale, Maria Nolano, Antonino Uncini, Lucio Santoro.   

Abstract

Some evidences highlighted a higher clinical expression of hereditary neuropathy with liability to pressure palsy (HNPP) in males, and a higher load of traumatic nerve injuries due to different occupational activity has been invoked to explain this observation. It is unknown whether this increased clinical impairment corresponds to a greater electrophysiological involvement. Thus, we compared clinical and electrophysiological features between men and women in a large cohort of HNPP patients. Nerve palsies and electrophysiological abnormalities were more frequent in men, and electrophysiological findings which differentiated males from females did not show any age-related worsening. In conclusion, our findings showed a higher clinical and electrophysiological involvement in males which does not seem related to different cumulative nerve damage over time. We believe that the higher disease expression may increase the chance to detect the disease in males and, thereby, to underestimate the HNPP diagnosis in females.

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Year:  2012        PMID: 23207550     DOI: 10.1007/s10072-012-1258-8

Source DB:  PubMed          Journal:  Neurol Sci        ISSN: 1590-1874            Impact factor:   3.307


  10 in total

1.  Electrodiagnostic features of hereditary neuropathy with liability to pressure palsies.

Authors:  P B Andersson; E Yuen; K Parko; Y T So
Journal:  Neurology       Date:  2000-01-11       Impact factor: 9.910

2.  Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion.

Authors:  J Infante; A García; O Combarros; J I Mateo; J Berciano; M J Sedano; E J Gutiérrez-Rivas; F Palau
Journal:  Muscle Nerve       Date:  2001-09       Impact factor: 3.217

3.  Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion.

Authors:  P Mouton; S Tardieu; R Gouider; N Birouk; T Maisonobe; O Dubourg; A Brice; E LeGuern; P Bouche
Journal:  Neurology       Date:  1999-04-22       Impact factor: 9.910

4.  Age associated axonal features in HNPP with 17p11.2 deletion in Japan.

Authors:  H Koike; M Hirayama; M Yamamoto; H Ito; N Hattori; F Umehara; K Arimura; S Ikeda; Y Ando; M Nakazato; R Kaji; K Hayasaka; M Nakagawa; S Sakoda; K Matsumura; O Onodera; M Baba; H Yasuda; T Saito; J Kira; K Nakashima; N Oka; G Sobue
Journal:  J Neurol Neurosurg Psychiatry       Date:  2005-08       Impact factor: 10.154

5.  Conduction block in PMP22 deficiency.

Authors:  Yunhong Bai; Xuebao Zhang; Istvan Katona; Mario Andre Saporta; Michael E Shy; Heather A O'Malley; Lori L Isom; Ueli Suter; Jun Li
Journal:  J Neurosci       Date:  2010-01-13       Impact factor: 6.167

6.  Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion.

Authors:  R Gouider; E LeGuern; M Gugenheim; S Tardieu; T Maisonobe; J M Léger; J M Vallat; Y Agid; P Bouche; A Brice
Journal:  Neurology       Date:  1995-11       Impact factor: 9.910

7.  Clinical spectrum of the tomaculous neuropathies. Report of 60 cases and review of the literature.

Authors:  N Rizzuto; G Moretto; S Galiazzo Rizzuto
Journal:  Ital J Neurol Sci       Date:  1993-12

8.  Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A).

Authors:  Michael W Sereda; Gerd Meyer zu Hörste; Ueli Suter; Naureen Uzma; Klaus-Armin Nave
Journal:  Nat Med       Date:  2003-11-09       Impact factor: 53.440

9.  Hereditary neuropathy with liability to pressure palsy: the electrophysiology fits the name.

Authors:  Jun Li; Karen Krajewski; Michael E Shy; Richard A Lewis
Journal:  Neurology       Date:  2002-06-25       Impact factor: 9.910

10.  Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication.

Authors:  A Uncini; G Di Guglielmo; A Di Muzio; D Gambi; M Sabatelli; T Mignogna; P Tonali; R Marzella; P Finelli; N Archidiacono
Journal:  Muscle Nerve       Date:  1995-06       Impact factor: 3.217

  10 in total
  3 in total

Review 1.  Hereditary neuropathy with liability to pressure palsies.

Authors:  Shahram Attarian; Farzad Fatehi; Yusuf A Rajabally; Davide Pareyson
Journal:  J Neurol       Date:  2019-04-15       Impact factor: 4.849

2.  Charcot-Marie-Tooth disease: genetic subtypes in the Sardinian population.

Authors:  Lorena Lorefice; Maria Rita Murru; Giancarlo Coghe; Giuseppe Fenu; Daniela Corongiu; Jessica Frau; Stefania Tranquilli; Paolo Tacconi; Alessandro Vannelli; Giovanni Marrosu; Elena Mamusa; Eleonora Cocco; Maria Giovanna Marrosu
Journal:  Neurol Sci       Date:  2017-03-13       Impact factor: 3.307

Review 3.  New evidence for secondary axonal degeneration in demyelinating neuropathies.

Authors:  Kathryn R Moss; Taylor S Bopp; Anna E Johnson; Ahmet Höke
Journal:  Neurosci Lett       Date:  2020-12-24       Impact factor: 3.046

  3 in total

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