Literature DB >> 8386695

Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern Quebec.

M De Braekeleer1, A Dallaire, J Mathieu.   

Abstract

Sensorimotor polyneuropathy with or without agenesis of the corpus callosum (McKusick number 218000) is a disorder that has a high frequency in Saguenay-Lac-St-Jean (SLSJ), a geographically isolated region of north-eastern Quebec. The incidence at birth and the carrier rate were estimated, respectively, at 1/2117 liveborns and 1/23 inhabitants. Remote consanguinity was found in several polyneuropathic families while the mean kinship coefficient was 2.7 times higher in the polyneuropathic group than in control groups. The birth places of the individuals with sensorimotor polyneuropathy and their parents did not show a clustered nonuniform distribution. The genealogical reconstruction suggests that the high incidence of polyneuropathy in SLSJ is likely to be the result of a founder effect. It also suggests that a unique mutation accounts for most, if not all, of the cases of sensorimotor polyneuropathy known in this region.

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Year:  1993        PMID: 8386695     DOI: 10.1007/bf00218260

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  13 in total

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  6 in total

Review 1.  Physiological roles and molecular mechanisms of K+ -Cl- cotransport in the mammalian kidney and cardiovascular system: where are we?

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Journal:  J Physiol       Date:  2019-02-09       Impact factor: 5.182

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Authors:  Tania Cruz Marino; Jessica Tardif; Josianne Leblanc; Janie Lavoie; Pascal Morin; Michel Harvey; Marie-Jacqueline Thomas; Annabelle Pratte; Nancy Braverman
Journal:  Hum Genet       Date:  2021-08-13       Impact factor: 4.132

3.  The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q.

Authors:  L K Casaubon; M Melanson; I Lopes-Cendes; C Marineau; E Andermann; F Andermann; J Weissenbach; C Prévost; J P Bouchard; J Mathieu; G A Rouleau
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

4.  A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.

Authors:  Sebastien Levesque; Charles Morin; Simon-Pierre Guay; Josee Villeneuve; Pascale Marquis; Wing Yan Yik; Sarn Jiralerspong; Luigi Bouchard; Steven Steinberg; Joseph G Hacia; Ken Dewar; Nancy E Braverman
Journal:  BMC Med Genet       Date:  2012-08-15       Impact factor: 2.103

5.  Temporal manipulation of KCC3 expression in juvenile or adult mice suggests irreversible developmental deficit in hereditary motor sensory neuropathy with agenesis of the corpus callosum.

Authors:  Bianca Flores; Eric Delpire
Journal:  Am J Physiol Cell Physiol       Date:  2021-02-17       Impact factor: 5.282

6.  Exome sequencing study of partial agenesis of the corpus callosum in men with developmental delay, epilepsy, and microcephaly.

Authors:  Jolyane Meloche; Vanessa Brunet; Pierre-Alexandre Gagnon; Marie-Ève Lavoie; Jean-Benoît Bouchard; Javad Nadaf; Jacek Majewski; Charles Morin; Catherine Laprise
Journal:  Mol Genet Genomic Med       Date:  2019-10-02       Impact factor: 2.183

  6 in total

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