Literature DB >> 1638075

Menkes' disease: report of a case and determination of eumelanin and pheomelanin in hypopigmented hair.

Y Tomita1, Y Kondo, S Ito, M Hara, T Yoshimura, H Igarashi, H Tagami.   

Abstract

We report a male infant with Menkes' disease who showed, at the age of 3 months, slow growth, hair abnormalities such as pili torti and white hair, and low levels of serum copper and ceruloplasmin. The exceptionally bright portions of his hair contained eumelanin and pheomelanin at levels only half those of normal Japanese controls. After subcutaneous administration of copper-histidinate for 2 months, his scalp hair changed to dark brown.

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Year:  1992        PMID: 1638075     DOI: 10.1159/000247407

Source DB:  PubMed          Journal:  Dermatology        ISSN: 1018-8665            Impact factor:   5.366


  2 in total

1.  Focal Scalp Hair Heterochromia in an Infant.

Authors:  Pramod Kumar
Journal:  Sultan Qaboos Univ Med J       Date:  2017-03-30

2.  Epidemiological and investigative study of premature graying of hair in higher secondary and pre-university school children.

Authors:  Ramesh M Bhat; Rashmi Sharma; Anita C Pinto; Sukumar Dandekeri; Jacintha Martis
Journal:  Int J Trichology       Date:  2013-01
  2 in total

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