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Menkes kinky-hair disease. A report on its pathology

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Summary

Two cases of Menkes disease belonging to different families are reported in order to illustrate different types of central nervous system involvement. In the first case which documents the sex-linked recessive inheritance, arteriographic studies have shown that the vascularization of the brain was severely impaired. Postmortem examination revealed lesions of the elastic membranes of large and medium calibre arteries, widespread and extremely severe necroses of grey and white matter with relative sparing of the territories irrigated by the vertebro-basilar system. The dendritic tree of the Purkinje cells was atrophied, somal sprouts were not found. Electron microscopy showed the mitochondria to be morphologically normal. In the second case, there was a bilateral demyelination predominating in the temporal lobes' white matter while arterial alterations and anoxic lesions were present but less prominent. The Purkinje cells were normal.

Considering the role of copper as a co-factor for different enzymes, it is possible to explain many features of Menkes disease on the basis of a lack of copper (Danks et al., 1972a, b). Multiple elements play a role in the pathogenesis of the C.N.S. lesions: some alterations, such as the parenchymatous necroses, depend from circulatory disturbances related to arterial abnormalities; others, such as the demyelination, the dystrophic features etc., could be linked to various enzymatic deficiencies susceptible to interfere with postnatal myelination and differentiation of cell membranes as illustrated by the study of spontaneous and experimental animal diseases.

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References

  • Aguilar, M. J., Chadwick, D. L., Okuyama, K., Kamoshita, S.: Kinky hair disease. I. Clinical and pathological features. J. Neuropath. exp. Neurol.25, 507–522 (1966)

    Article  CAS  PubMed  Google Scholar 

  • Barlow, R. M., Cancilla, P. A.: Structural changes of the central nervous system in swayback (enzootic ataxia) of lambs. I. Light microscopy using phosphatases as organelle markers. Acta neuropath. (Berl.)6, 175–180 (1966)

    Article  Google Scholar 

  • Boyde, A., Wood, C.: Preparation of animal tissue for surface-scanning electron microscopy. J. Microscopy90, 221–249 (1969)

    Article  CAS  Google Scholar 

  • Cancilla, P. A., Barlow, R. M.: Structural changes of the central nervous system in swayback (enzootic ataxia) of lambs. II. Electron microscopy of the lower motor neuron. Acta neuropath. (Berl.)6, 251–259 (1966a)

    Article  CAS  Google Scholar 

  • Cancilla, P. A., Barlow, R. M.: Structural changes of the central nervous system in swayback (enzootic ataxia) of lambs. III. Electron microscopy of the cerebral lesions. Acta neuropath. (Berl.)6, 260–265 (1966b).

    Article  CAS  Google Scholar 

  • Cancilla, P. A., Barlow, R. M.: Structural changes of the central nervous system in swayback (enzootic ataxia) of lambs. IV. Electron microscopy of the white matter of the spinal cord. Acta neuropath. (Berl.)11, 294–300 (1968)

    Article  CAS  Google Scholar 

  • Cancilla, P. A., Barlow, R. M.: Structural changes of the central nervous system in swayback (enzootic ataxia) of lambs. V. Electron microscopic observations of the corpus callosum. Acta neuropath. (Berl.)12, 307–313 (1969)

    Article  CAS  Google Scholar 

  • Cancilla, P. A., Barlow, R. M.: Experimental copper deficiency in miniature swine. Biochemistry, histochemistry and pathology of the central nervous system. J. comp. Path.80, 315–319 (1970)

    Article  CAS  PubMed  Google Scholar 

  • Danks, D. M., Cartwright, E., Stevens, B. J., Townley, R. R. W.: Menkes' kinky hair disease: further definition of the defect in copper transport. Science179, 1140–1142 (1973)

    Article  CAS  PubMed  Google Scholar 

  • Danks, D. M., Campbell, P. E., Stevens, B. J., Mayne, V., Cartwright, E.: Menkes's kinky hair syndrome. An inherited defect in copper absorption with widespread effects. Pediatrics50, 188–201 (1972a)

    CAS  PubMed  Google Scholar 

  • Danks, D. M., Stevens, B. J., Campbell, P. E., Gillespie, J. M., Walker-Smith, J., Blomfield, J., Turner, B.: Menkes' kinky hair syndrome. LancetI, 1100–1103 (1972b)

    Article  Google Scholar 

  • DiPaolo, R. V., Kanfer, J. N., Newberne, P. M.: Copper deficiency and the central nervous system. Myelination in the rat: morphological and biochemical studies. J. Neuropath. exp. Neurol.33, 226–236 (1974)

    Article  CAS  PubMed  Google Scholar 

  • French, J. H., Sherard, E. S., Lubell, H., Brotz, M., Moore, C. L.: Trichopoliodystrophy. I. Report of a case and biochemical studies. Arch. Neurol. (Chic.)26, 229–244 (1972)

    Article  CAS  Google Scholar 

  • Ghatak, N. R., Hirano, A., Poon, T. P., French, J. H.: Trichopoliodystrophy. II. Pathological changes in skeletal muscle and nervous system. Arch. Neurol. (Chic.)26, 60–72 (1972)

    Article  CAS  Google Scholar 

  • Goka, T. J., Stevenson, R. E., Hefferan, P. M., Howell, R. R.: Menkes' disease: a biochemical abnormality in cultured human fibroblasts. Proc. Nat. Acad. Sci. (U.S.A.)73, 604–606 (1976)

    Article  CAS  Google Scholar 

  • Hirano, A., Llena, J. F., French, J. H., Ghatak, N. R.: Fine structure of the cerebellar cortex in Menkes' kinky hair disease. X-chromosome-linked copper malabsorption. Arch. Neurol. (Chic.)34, 52–56 (1977)

    Article  CAS  Google Scholar 

  • Horn, N.: Copper incorporation studies on cultured cells for prenatal diagnosis of Menkes' disease. LancetI, 1156–1158 (1976)

    Article  Google Scholar 

  • Horn, N., Warburg, M.: Menkes' disease. Birth Defects: Original Article Series, Vol. XII, No. 3., 557–562, The National Foundation (1976)

    Google Scholar 

  • Hunt, D. M.: Primary defect in copper transport underlies mottled mutants in the mouse. Nature249, 852–854 (1974)

    Article  CAS  PubMed  Google Scholar 

  • Hunt, D. M., Johnson, D. R.: Aromatic amino-acid metabolism in brindled (Mobr) and Viable-brindled (Movbr) two alleles at the mottled locus in the mouse. Biochem. Genetics6, 31–40 (1972a)

    Article  CAS  Google Scholar 

  • Hunt, D. M., Johnson, D. R.: An inherited deficiency in noradrenaline biosynthesis in the brindled mouse. J. Neurochem.19, 2811–2819 (1972b)

    Article  CAS  PubMed  Google Scholar 

  • Kopp, N., Tommasi, M., Carrier, H., Pialat, J., Gilly, J., Herve, C.: Neuropathologie de la trichopoliodystrophie (maladie de Menkes). Une observation anatomo-clinique. Rev. neurol. (Paris)131, 775–789 (1975)

    CAS  Google Scholar 

  • Lott, I. T., DiPaolo, R., Schwartz, D., Jonowska, S., Kanfer, J. N.: Copper metabolism in the steely-hair syndrome. New Engl. J. Med.292, 197–198 (1975)

    Article  CAS  PubMed  Google Scholar 

  • Martin, J. J., Schlote, W.: Central nervous system lesions in disorders of amino-acid metabolism. A neuropathological study. J. neurol. Sci.15, 49–76 (1972)

    Article  CAS  PubMed  Google Scholar 

  • Martin, J. J., de Barsy, Th., Van Hoof, F., Palladini, G.: Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle. Acta neuropath. (Berl.)23, 229–244 (1973)

    Article  CAS  Google Scholar 

  • Martin, J. J., Leroy, J. G., Farriaux, J. P., Fontaine, G., Desnick, R. J., Cabello, A.: I-cell disease (Mucolipidosis II). A report on its pathology. Acta neuropath. (Berl.)33, 285–305 (1975)

    Article  CAS  Google Scholar 

  • Menkes, J. H., Alter, M., Steigleder, G. K., Weakley, D. R., Sung, J. H.: A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration. Peidiatrics29, 764–779 (1962)

    CAS  Google Scholar 

  • Morgan, R. F., O'Dell, B. L.: Effect of copper deficiency on the concentrations of catecholamines and related enzyme activities in the rat brain. J. Neurochem.28, 207–213 (1977)

    Article  CAS  PubMed  Google Scholar 

  • Nyström, S. H. M.: Studies of the effect of experimental hypocupremia on the rabbit circulatory system, with special reference to the vessels of the neck and the base of the brain. Acta neuropath. (Berl.)10, 209–217 (1968)

    Article  Google Scholar 

  • Oakes, B. W., Danks, D. M., Campbell, P. E.: Human copper deficiency: Ultrastructural studies of the aorta and skin in a child with Menkes' syndrome. Exp. molecul. Path.25, 82–98 (1976)

    Article  CAS  Google Scholar 

  • O'Dell, B. L., Smith, R. M., King, R. A.: Effect of copper status on brain neurotransmitter metabolism in the lamb. J. Neurochem.26, 451–455 (1976)

    Article  PubMed  Google Scholar 

  • Osaka, K., Sato, N., Matsumoto, S., Ogino, H., Kodama, S., Yokoyama, S., Sugiyama, T.: Congenital hypocupraemia syndrome with and without steely hair: Report of two Japanese infants. Develop. Med. Child Neurol.19, 62–68 (1977)

    Article  CAS  PubMed  Google Scholar 

  • Prohaska, J. R., Wells, W. W.: Copper deficiency in the developing rat brain: A possible model for Menkes's steely-hair disease. J. Neurochem.23, 91–98 (1974)

    Article  CAS  PubMed  Google Scholar 

  • Prohaska, J. R., Wells, W. W.: Copper deficiency in the developing rat brain: Evidence for abnormal mitochondria. J. Neurochem.25, 221–228 (1975)

    Article  CAS  PubMed  Google Scholar 

  • Purpura, D. P., Hirano, A., French, J. H.: Polydendritic Purkinje cells in X-chromosome linked copper malabsorption: a Golgi study. Brain Res.117, 125–129 (1976)

    Article  CAS  PubMed  Google Scholar 

  • Reske-Nielsen, E., Lou, H. C., Vagn-Hansen, P. L.: Menkes' disease. A hypothesis with recommendations for future investigations. Acta neuropath. (Berl.)28, 361–363 (1974)

    Article  CAS  Google Scholar 

  • Rochiccioli, P., Dutau, G., Delsol, G., Ghisolfi, J., Augier, D.: Le syndrome de Menkes. Etude clinique, métabolique et ultrastructurale. Arch. franç. Pédiat.30, 209 (1973)

    Google Scholar 

  • Spaïs, A., Palsson, P. A., van Bogaert, L.: Pathology of enzootic ataxia of lambs (sway-back). Acta neuropath. (Berl.)1, 56–72 (1961)

    Article  Google Scholar 

  • tilmont, P.: La maladie de Menkes (Trichopoliodystrophie). Thèse de doctorat en médecine-Université de Lille, 1974 pages, 1977

  • Vagn-Hansen, P. L., Reske-Nielsen, E., Lou, H. C.: Menkes' disease. A clinical and neuropathological review together with a new case. Acta neuropath. (Berl.)25, 103–119 (1973)

    Article  CAS  Google Scholar 

  • Vuia, O., Heye, D.: Neuropathologic aspects in Menkes' kinky hair disease (trichopoliodystrophy). Neuropädiatrie5, 329–339 (1974)

    Article  CAS  PubMed  Google Scholar 

  • Wray, S. H., Kuwabara, T., Sanderson, P.: Menkes' kinky hair disease: A light and electron microscopic study of the eye. Invest. Ophthal.15, 128–138 (1976)

    CAS  PubMed  Google Scholar 

  • Zimmerman, A. W., Matthieu, J.-M., Quarles, R. H., Brady, R. O., Hsu, J. M.: Hypomyelination in copper-deficient rats. Prenatal and postnatal copper replacement. Arch. Neurol. (Chic.)33, 111–119 (1976)

    Article  CAS  Google Scholar 

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Martin, J.J., Flament-Durand, J., Farriaux, J.P. et al. Menkes kinky-hair disease. A report on its pathology. Acta Neuropathol 42, 25–32 (1978). https://doi.org/10.1007/BF01273263

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