Menkes Kinky-Hair Syndrome (Trichopoliodystrophy)
- 1 April 1973
- journal article
- research article
- Published by American Medical Association (AMA) in American Journal of Diseases of Children
- Vol. 125 (4) , 572-578
- https://doi.org/10.1001/archpedi.1973.04160040072015
Abstract
Kinky-hair syndrome, a progressive neurodegenerative disorder which affects infant males and is characterized by unusual hair, seizures, psychomotor retardation, growth failure, and early death, was first described by Menkes et al.1 Since the original description, 11 more cases have been reported from this country.2 Additional features, including bone changes and tortuous cerebral vessels, have been noted subsequently. Recently Danks et al,3 from Australia, have reported very low levels of copper and copper oxidase in the blood in five cases. Poor absorption of copper was thought to be the mechanism involved, although this was not proven. This paper presents a new case of kinky-hair syndrome showing typical clinical and radiological features and very low copper levels in the blood, urine, and hair. Relevant literature in relation to copper deficiency in man and animals is reviewed.Keywords
This publication has 6 references indexed in Scilit:
- Neonatal Copper DeficiencyNew England Journal of Medicine, 1971
- Copper MetabolismThe American Journal of Clinical Nutrition, 1969
- Radiological Findings in the Kinky-Hair SyndromeRadiology, 1969
- Chemical and Morphological Changes in the Brains of Copper-deficient Guinea PigsJournal of Nutrition, 1968
- The State of Copper in Human Serum: Evidence for an Amino Acid-bound Fraction *Journal of Clinical Investigation, 1967
- The Isolation and Properties of Some Soluble Proteins From Wool VIII. The Proteins of Copper-Deficient WoolAustralian Journal of Biological Sciences, 1964