Literature DB >> 8229500

Copper-histidine therapy for Menkes disease.

B Sarkar1, K Lingertat-Walsh, J T Clarke.   

Abstract

Menkes disease is an X-linked genetic disorder of copper transport that results in death from severe progressive neurodegeneration by the age of 3 years. We report here our 17 years' experience with the treatment of Menkes disease with subcutaneous administration of copper-histidine. Two patients (16 and 6 years of age) whose therapy was begun within 1 month of birth have done well neurologically. The other five patients have done poorly despite treatment initiated at 2 to 7 months of age. Copper-histidine therapy may be an effective treatment if started early.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8229500     DOI: 10.1016/s0022-3476(05)80870-4

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  14 in total

Review 1.  Menkes disease: recent advances and new aspects.

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

2.  Disulfiram enhanced delivery of orally administered copper into the central nervous system in Menkes disease mouse model.

Authors:  Takao Hoshina; Satoshi Nozaki; Takashi Hamazaki; Satoshi Kudo; Yuka Nakatani; Hiroko Kodama; Haruo Shintaku; Yasuyoshi Watanabe
Journal:  J Inherit Metab Dis       Date:  2018-08-21       Impact factor: 4.982

Review 3.  Genes of the copper pathway.

Authors:  D W Cox
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025

4.  Screening for Menkes disease using the urine HVA/VMA ratio.

Authors:  M Matsuo; R Tasaki; H Kodama; Y Hamasaki
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

Review 5.  Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes.

Authors:  P de Bie; P Muller; C Wijmenga; L W J Klomp
Journal:  J Med Genet       Date:  2007-08-23       Impact factor: 6.318

Review 6.  Copper transporting P-type ATPases and human disease.

Authors:  Diane W Cox; Steven D P Moore
Journal:  J Bioenerg Biomembr       Date:  2002-10       Impact factor: 2.945

7.  Effect of copper and diethyldithiocarbamate combination therapy on the macular mouse, an animal model of Menkes disease.

Authors:  H Kodama; E Sato; Y-H Gu; K Shiga; C Fujisawa; T Kozuma
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.750

Review 8.  Inherited copper transport disorders: biochemical mechanisms, diagnosis, and treatment.

Authors:  Hiroko Kodama; Chie Fujisawa; Wattanaporn Bhadhprasit
Journal:  Curr Drug Metab       Date:  2012-03       Impact factor: 3.731

9.  Overexpression of the RNA-binding proteins Lin28B and IGF2BP3 (IMP3) is associated with chemoresistance and poor disease outcome in ovarian cancer.

Authors:  K-F Hsu; M-R Shen; Y-F Huang; Y-M Cheng; S-H Lin; N-H Chow; S-W Cheng; C-Y Chou; C-L Ho
Journal:  Br J Cancer       Date:  2015-07-09       Impact factor: 7.640

10.  A Modular Ionophore Platform for Liver-Directed Copper Supplementation in Cells and Animals.

Authors:  Timothy A Su; Diyala S Shihadih; Wendy Cao; Tyler C Detomasi; Marie C Heffern; Shang Jia; Andreas Stahl; Christopher J Chang
Journal:  J Am Chem Soc       Date:  2018-10-15       Impact factor: 16.383

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.