Literature DB >> 1341968

Menkes disease: an X-linked neurological disorder of the copper metabolism.

N Horn1, T Tønnesen, Z Tümer.   

Abstract

Menkes disease is an X-linked, recessive disturbance of copper metabolism associated with a progressive clinical course and abnormal hair. The disease is dominated by neurological symptoms combined with connective tissue manifestations, most of which can be explained by the lack of important copper enzymes. Despite excessive accumulation of the metal in various tissues, a functional copper deficiency is evident, probably caused by a defective intracellular copper transport protein of unknown nature. The molecular basis of the copper disturbance has proven difficult to define and will most likely have to await cloning of the gene. The chromosomal region of interest has now been narrowed down to a sub-band on the long arm of the chromosome (Xq13.3), and positional cloning is in progress in a number of laboratories including our own. Identification of the Menkes gene will be of importance for our understanding of the cellular handling of copper and other trace elements.

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Year:  1992        PMID: 1341968     DOI: 10.1111/j.1750-3639.1992.tb00711.x

Source DB:  PubMed          Journal:  Brain Pathol        ISSN: 1015-6305            Impact factor:   6.508


  14 in total

1.  Abnormalities of copper accumulation in cell lines established from nine different alleles of mottled are the same as those found in Menkes disease.

Authors:  W Masson; H Hughes; D Papworth; Y Boyd; N Horn
Journal:  J Med Genet       Date:  1997-09       Impact factor: 6.318

2.  Identification of point mutations in 41 unrelated patients affected with Menkes disease.

Authors:  Z Tümer; C Lund; J Tolshave; B Vural; T Tønnesen; N Horn
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

Review 3.  Menkes disease: recent advances and new aspects.

Authors:  Z Tümer; N Horn
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

Review 4.  Copper-dependent functions for the prion protein.

Authors:  David R Brown; Judyth Sassoon
Journal:  Mol Biotechnol       Date:  2002-10       Impact factor: 2.695

5.  Cerebellar superoxide dismutase expression in Menkes' kinky hair disease: an immunohistochemical investigation.

Authors:  N Shibata; A Hirano; M Kobayashi; T Umahara; T Kawanami; K Asayama
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

6.  Detection of genetic defects in Menkes disease by direct mutation analysis and its implications in carrier diagnosis.

Authors:  Z Tümer; T Tønnesen; N Horn
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

7.  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

8.  The use of compound heterozygotes and Hprt selection to analyze X-linked mottled alleles associated with prenatal lethality.

Authors:  W Masson; S Holt; V Reed; Y Boyd
Journal:  Mamm Genome       Date:  1996-07       Impact factor: 2.957

9.  Clinical and biochemical consequences of copper-histidine therapy in Menkes disease.

Authors:  J Kreuder; A Otten; H Fuder; Z Tümer; T Tønnesen; N Horn; D Dralle
Journal:  Eur J Pediatr       Date:  1993-10       Impact factor: 3.183

10.  First trimester prenatal diagnosis of Menkes disease by DNA analysis.

Authors:  Z Tümer; T Tønnesen; J Böhmann; W Marg; N Horn
Journal:  J Med Genet       Date:  1994-08       Impact factor: 6.318

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