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Neurocutaneous Disorder and Mental Functioning

The Blake Marsh Lecture for 1974, delivered before the Royal College of Psychiatrists, 4 February 1974

Published online by Cambridge University Press:  29 January 2018

J. Jancar
J. Jancar*
Affiliation:
Stoke Park Group Hospitals and University of Bristol; Stoke Park Hospital, Stapleton, Bristol, BS16 1QU
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Extract

Disorders of the skin, either congenital or acquired, associated with nervous disorders and disturbance of normal mental functioning arc numerous. The classification is very wide-ranging and includes: phakomatoses, hamartoses, adenomatoses and neurocutaneous syndromes. In 1972, Liebaldt and Leiber collected 40 titles of the syndromes, and since then many more reports of the new syndromes and their variants have appeared in the world literature.

Type
Research Article
Information
The British Journal of Psychiatry , Volume 126 , Issue 2 , February 1975 , pp. 105 - 113
Copyright
Copyright © Royal College of Psychiatrists, 1975 

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References

Alexander, G. L. & Norman, R. M. (1960) The Sturge-Weber Syndrome. Bristol: John Wright and Sons Ltd.Google Scholar
Arseni, C., Alexianu, M., Horvat, L., Alexianu, D. & Petrovici, Al. (1972) Fine structure of atypical cells in tuberous sclerosis. Acta Neuropathologica (Berl.), 21, 185–93.CrossRefGoogle ScholarPubMed
Beveridge, G. W. (1974) Diseases of the skin—infantile eczema. British Medical Journal, i, 154–5.Google Scholar
Carney, R. G. & Carney, R. G. Jr. (1970) Incontinentia pigmenti. Archives of Dermatology, 102, 157–62.Google Scholar
Cleaver, J. E. (1970) DNA damage and repair in light-sensitive human skin diseases. Journal of Investigative Dermatology, 54, 181–95.CrossRefGoogle Scholar
Copeman, P. W. M. (1974) Diseases of the skin—Drug ill effects on the skin. British Medical Journal, i, 110–13.CrossRefGoogle ScholarPubMed
Dean, G. (1971) The Porphyrias: A Story of Inheritance and Environment. 2nd edn. London: Pitman Medical.Google Scholar
Eastham, R. D. & Jancar, J. (1968) Clinical Pathology in Mental Retardation. Bristol: John Wright & Sons Ltd.Google Scholar
Eastham, R. D. (1969) Macrocytosis in Down's syndrome. Lancet, i, 895.Google Scholar
Eastham, R. D. (1971) Epilepsy and folate deficiency. British Medical Journal, iv, 361–2.Google Scholar
Hamilton, W. J. & Mossman, H. W. (1972) Human Embryology . Prenatal Development of Form and Function. Fourth ed. Cambridge: W. Heffer & Sons Ltd.Google Scholar
Hurwitz, S. & Braverman, I. M. (1970) White spots in tuberous sclerosis. Journal of Pediatrics, 77, 587–94.CrossRefGoogle ScholarPubMed
Jancar, J. (1969) Pellagra like reaction due to PAS and isoniazid treatment. Journal of Mental Subnormality, 15, 100–103.Google Scholar
Jancar, J. (1970) Naevus syringocystadenomatosus papilliferus with skull and brain lesions, hemiparesis, epilepsy and mental retardation. British Journal of Dermatology, 82, 402–405.CrossRefGoogle ScholarPubMed
Jancar, J. (1970) Retinitis pigmentosa with mental retardation, deafness and XX/XO sex chromosomes. Journal of Mental Deficiency Research, 14, 269–73.Google Scholar
Jancar, J. (1970) Twins with mental retardation and physical abnormalities. Preliminary report. Acta Geneticae Medicae et Gemellologiae, 19, 311–14.CrossRefGoogle ScholarPubMed
Jancar, J. (1970) Nome's disease. Recessive, sex-linked, progressive, oculocerebral degeneration. Clinical Genetics, 1, 353–6.Google Scholar
Jancar, J. (1971) Assessment unit for the mentally retarded. Bristol Medico-Chirurgical Journal, 86, 27–33.Google ScholarPubMed
Jancar, J. & Wiley, , Yvonne, V. (1972) Lesch-Nyhan syndrome (familial hyperuricaemia). Abstract 2nd Conference of the European Teratology Society, Prague, May 1972, 45.Google Scholar
Jancar, J. & Walters, Ruth M. (1974) Tapeto-retinal degeneration in three mentally retarded sisters with other disorders in the family tree. Proceedings IV International Congress of Neurogenetics and Neuro-Ophthalmology, Rome, September 1973.Google Scholar
Kuhl, D. E., Bevilacqua, J. E., Mishkin, M. M. & Sanders, T. P. (1972) The brain scan in Sturge-Weber Syndrome. Radiology, 103, 621–6.CrossRefGoogle ScholarPubMed
Liebaldt, G. P. & Leiber, B. (1972) Cutaneous dysplasias associated with neurological disorders. Synopsis and differential diagnosis. In Handbook of Clinical Neurology, 14, 101 (ed. Vinken, P. J. & Bruyn, G. W.). Amsterdam: North-Holland Publishing Company; New York: American Elsevier Publishing Co. Inc.Google Scholar
MacGillivray, R. C. (1973) Personal communication.Google Scholar
Mehregan, A. H. & Pincus, H. (1965) Life history of organoid nevi. Special reference to nevus sebaceus of Jadassohn. Archives of Dermatology, 91, 574–88.CrossRefGoogle ScholarPubMed
Moll, J. M. H. (1974) Psoriatic spondylitis: Clinical, radiological and familial aspects. Proceedings of the Royal Society of Medicine, 67, 46–50.CrossRefGoogle ScholarPubMed
Mori, M., Ikeda, T. & Onoe, T. (1971) Blastic Schwann cells in renal tumor of tuberous sclerosis complex. Acta Pathologica Japonica, 21(1), 121–9.Google Scholar
Noriega-Sanchez, A., Markand, O. N. & Herndon, J. H. (1972) Oculocutaneous melanosis associated with the Sturge-Weber syndrome. Neurology, 22, 256–62.CrossRefGoogle ScholarPubMed
Smith, C. (1972) Computer programme to estimate recurrence risk for multifactorial familial disease. British Medical Journal, i, 495–7.Google Scholar
Waldmann, T. A. & McIntire, K. R. (1972) Serumalpha-fetoprotein levels in patients with ataxia-telangiectasia. Lancet, ii, 1112–5.Google Scholar
Whitehouse, D. (1966) Diagnostic value of the café-aulait spot in children. Archives of Disease in Childhood, 41, 316–9.CrossRefGoogle Scholar
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