Literature DB >> 7687955

Spectrum of EEG findings in Menkes disease.

S R White1, K Reese, S Sato, S G Kaler.   

Abstract

We evaluated electroencephalograms (EEGs) in 10 boys with Menkes disease, ranging in age from 9 days to 27 months. Three of 10 tracings were normal (the newborn, his 27-month-old half-brother with the classic phenotype, and a 27-month-old mildly affected patient). Plasma copper levels were low in all patients except the newborn and tended to be lowest in patients whose EEGs were moderately or severely abnormal. EEG differences in Menkes patients could reflect biochemical and molecular heterogeneity with respect to copper availability and utilization in the brain.

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Year:  1993        PMID: 7687955     DOI: 10.1016/0013-4694(93)90175-u

Source DB:  PubMed          Journal:  Electroencephalogr Clin Neurophysiol        ISSN: 0013-4694


  16 in total

Review 1.  ATP7A-related copper transport diseases-emerging concepts and future trends.

Authors:  Stephen G Kaler
Journal:  Nat Rev Neurol       Date:  2011-01       Impact factor: 42.937

2.  Diagnosis of copper transport disorders.

Authors:  Lisbeth B Møller; Julia D Hicks; Courtney S Holmes; David S Goldstein; Cornelia Brendl; Peter Huppke; Stephen G Kaler
Journal:  Curr Protoc Hum Genet       Date:  2011-07

3.  Identification of a novel mutation in the ATP7A gene in a Korean patient with Menkes disease.

Authors:  Yong Hyuk Kim; Ran Lee; Han Wook Yoo; Mi-Sun Yum; Sun Hwan Bae; So Chung Chung; Yong Mean Park; Jae Sung Son
Journal:  J Korean Med Sci       Date:  2011-06-20       Impact factor: 2.153

Review 4.  Inborn errors of copper metabolism.

Authors:  Stephen G Kaler
Journal:  Handb Clin Neurol       Date:  2013

5.  Molecular correlates of epilepsy in early diagnosed and treated Menkes disease.

Authors:  Stephen G Kaler; Clarissa J Liew; Anthony Donsante; Julia D Hicks; Susumu Sato; Jacquelyn C Greenfield
Journal:  J Inherit Metab Dis       Date:  2010-07-21       Impact factor: 4.982

6.  Somatic mosaicism in Menkes disease suggests choroid plexus-mediated copper transport to the developing brain.

Authors:  Anthony Donsante; Paul Johnson; Laura A Jansen; Stephen G Kaler
Journal:  Am J Med Genet A       Date:  2010-10       Impact factor: 2.802

7.  L-threo-dihydroxyphenylserine corrects neurochemical abnormalities in a Menkes disease mouse model.

Authors:  Anthony Donsante; Patricia Sullivan; David S Goldstein; Lauren R Brinster; Stephen G Kaler
Journal:  Ann Neurol       Date:  2012-12-07       Impact factor: 10.422

8.  Differences in ATP7A gene expression underlie intrafamilial variability in Menkes disease/occipital horn syndrome.

Authors:  Anthony Donsante; Jingrong Tang; Sarah C Godwin; Courtney S Holmes; David S Goldstein; Alexander Bassuk; Stephen G Kaler
Journal:  J Med Genet       Date:  2007-05-11       Impact factor: 6.318

Review 9.  Translational research investigations on ATP7A: an important human copper ATPase.

Authors:  Stephen G Kaler
Journal:  Ann N Y Acad Sci       Date:  2014-04-15       Impact factor: 5.691

10.  Clinical outcomes in Menkes disease patients with a copper-responsive ATP7A mutation, G727R.

Authors:  Jingrong Tang; Anthony Donsante; Vishal Desai; Nicholas Patronas; Stephen G Kaler
Journal:  Mol Genet Metab       Date:  2008-08-26       Impact factor: 4.797

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