Literature DB >> 3220711

Recurrent familial neuropathy due to liability to pressure palsies.

R Marazzi1, D Pareyson, V Scaioli, M Corbo, A Boiardi, G Chiodelli, A Sghirlanzoni.   

Abstract

Two families with hereditary neuropathy with liability to pressure palsies (HNPP) were evaluated clinically, electrophysiologically and pathologically (2 index cases). Familial patterns suggest autosomal dominant inheritance. The clinical presentation is characteristic, with recurrent painless transitory mononeuropathy, without evident triggering factors, or caused by trivial trauma or pressure. In affected members neurophysiological studies showed diffuse slowing in nerve conduction, more evident at common sites of entrapment. Somatosensory evoked potentials (SEPs) showed bilateral peripheral abnormalities with proximal nerve involvement more pronounced in older patients. 40 to 75% of teased fibers displayed sausage-shaped swellings. Ultrastructurally some sausages showed redundant myelin loops and excessive number of myelin lamellae that seem to cause axonal constriction.

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Year:  1988        PMID: 3220711     DOI: 10.1007/bf02333999

Source DB:  PubMed          Journal:  Ital J Neurol Sci        ISSN: 0392-0461


  13 in total

1.  Familial recurrent polyneuropathy. A family and a survey.

Authors:  D Roos; P Thygesen
Journal:  Brain       Date:  1972       Impact factor: 13.501

2.  Hereditary neuropathy with liability to pressure palsies. Electrophysiological and histopathological aspects.

Authors:  F Behse; F Buchthal; F Carlsen; G G Knappeis
Journal:  Brain       Date:  1972       Impact factor: 13.501

3.  Clinical and electroneuromyographical findings in hereditary neuropathy with liability to pressure palsies.

Authors:  W Görke
Journal:  Neuropadiatrie       Date:  1974-11

4.  Hereditary compression syndrome of peripheral nerves.

Authors:  A Staal; C J de Weerdt; L N Went
Journal:  Neurology       Date:  1965-11       Impact factor: 9.910

5.  Recurrent familial neuropathy with liability to pressure palsies: reports of two cases and ultrastructural nerve study.

Authors:  J Dubi; F Regli; A Bischoff; C Schneider; G de Crousaz
Journal:  J Neurol       Date:  1979-01-30       Impact factor: 4.849

6.  Peripheral and central conduction times in hereditary pressure-sensitive neuropathy.

Authors:  A Ebner; R Dengler; C Meier
Journal:  J Neurol       Date:  1981       Impact factor: 4.849

7.  [Hereditary neuropathy with a tendency to compression paralysis. Electrophysiological, morphometric and ultrastructural study of 2 familial cases].

Authors:  V Cavallari; M R Di Pasquale; D Scuderi
Journal:  Acta Neurol Quad (Napoli)       Date:  1981

8.  Hereditary pressure-sensitive neuropathy.

Authors:  J Debruyne; I Dehaene; J J Martin
Journal:  J Neurol Sci       Date:  1980-09       Impact factor: 3.181

9.  Brachial plexus involvement in familial pressure-sensitive neuropathy: electrophysiological and morphological findings.

Authors:  E P Bosch; H C Chui; M A Martin; P A Cancilla
Journal:  Ann Neurol       Date:  1980-12       Impact factor: 10.422

10.  Long-lasting conduction block in hereditary neuropathy with liability to pressure palsies.

Authors:  M R Magistris; G Roth
Journal:  Neurology       Date:  1985-11       Impact factor: 9.910

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  2 in total

1.  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

2.  A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.

Authors:  D Lorenzetti; D Pareyson; A Sghirlanzoni; B B Roa; N E Abbas; M Pandolfo; S Di Donato; J R Lupski
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

  2 in total

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