Literature DB >> 1322507

Hereditary neuropathy with liability to pressure palsies in childhood.

A A Gabreëls-Festen1, F J Gabreëls, E M Joosten, H M Vingerhoets, W O Renier.   

Abstract

Four children, index cases of families in which autosomal dominant neuropathy with liability to pressure palsies (HNPP) was diagnosed, are presented. Only one child was admitted for evaluation of an acute peroneal palsy, three presented with other symptoms. Polyneuropathy was diagnosed in all four children, in one of their parents and in some sibs. On inquiry, one child and several members of the four families had experienced transient palsies before. Morphological studies of the sural nerves showed frequently large tomacula and a neuropathic process of segmental de- and remyelination, and axonal degeneration. Attention is drawn to the atypical presentation without pressure palsies of HNPP.

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Year:  1992        PMID: 1322507     DOI: 10.1055/s-2008-1071329

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  4 in total

1.  Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1.

Authors:  E C Mariman; A A Gabreëls-Festen; S E van Beersum; P J Jongen; H H Ropers; F J Gabreëls
Journal:  Hum Genet       Date:  1993-08       Impact factor: 4.132

2.  Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith-Magenis syndrome with evident peripheral neuropathy.

Authors:  Bo Yuan; Juanita Neira; Shen Gu; Tamar Harel; Pengfei Liu; Ignacio Briceño; Sarah H Elsea; Alberto Gómez; Lorraine Potocki; James R Lupski
Journal:  Hum Genet       Date:  2016-07-07       Impact factor: 4.132

Review 3.  PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies.

Authors:  Barbara W van Paassen; Anneke J van der Kooi; Karin Y van Spaendonck-Zwarts; Camiel Verhamme; Frank Baas; Marianne de Visser
Journal:  Orphanet J Rare Dis       Date:  2014-03-19       Impact factor: 4.123

4.  Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene.

Authors:  Carlo Fusco; Carlotta Spagnoli; Grazia Gabriella Salerno; Elena Pavlidis; Daniele Frattini; Francesco Pisani
Journal:  Ital J Pediatr       Date:  2017-10-27       Impact factor: 2.638

  4 in total

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