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Age of Onset and Evolution of Fabry's Disease

Published online by Cambridge University Press:  01 August 2014

Albert Th. Franceschetti
Albert Th. Franceschetti*
Affiliation:
Department of Ophthalmology, University of Geneva, Switzerland
*
Clinique Universitaire d'Ophtalmologie, Hôpital Cantonal, Genève, Switzerland

Abstract

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Personal examination of 39 cases of Fabry's disease, with special respect to a chronogenetical analysis, revealed interesting temporal features both in the age of onset and the age of death.

Type
7. Free Contributions: Third Group
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 23 , supplement S1 , January 1974 , pp. 293 - 298
Copyright
Copyright © The International Society for Twin Studies 1974

References

BIBLIOGRAPHY

Christensen Lou, H.O. 1967. Fabry's disease. A clinical study with emphasis on neurological symptoms and signs. Second Int. Congr. Neuro-Ophthalmol., Montreal. Progress in Neuro-Ophthalmology. [pp. 363–376]. Amsterdam 1969: Excerpta Medica.Google Scholar
Christensen Lou, H.O., Heidensleben, E., Larsen, H.W. 1970. The value of ocular findings in the diagnosis of angiokeratoma corporis diffusum (Fabry's disease). Acta Ophthalmol. (Kbh.), 48: 1185–1194.Google Scholar
Denden, A., Franceschetti, A.Th. 1968. Cornea Verticillata: ein Symptom des Morbus Fabry-Anderson. Ber. Dtsch. Ophthalmol. Ges., 69:145–148.Google Scholar
Desnick, R.J., Simmons, R.L., Allen, K.Y., Woods, J.E., Anderson, C.F., Najarian, J.S., Krivit, W. 1972. Correction of enzymatic deficiencies by renal transplantation. Fabry's disease. Surgery, 72: 203–211.Google Scholar
Franceschetti, A.Th. 1967. La cornea verticillata et ses relations avec la maladie de Fabry (angiokeratoma corporis diffusum). Soc. Suisse Ophtalmol., Flims. Ophthalmologica, 156: 232–238, 1968.Google Scholar
Franceschetti, A.Th. 1973. Etude ophtalmologique, génétique et biochimique de la maladie de Fabry. Revue de la littérature et analyse de 39 cas personnels. Chronica Dermatologica (Roma), 4: 371–591.Google Scholar
Gemmingen, C. v., Kierland, R.R., Opitz, J.M. 1965. Angiokeratoma corporis diffusum (Fabry's disease). Arch. Dermatol., 91: 206–218.CrossRefGoogle Scholar
Gruber, M. 1946. « Cornea verticillata ». 2. Mitteilung. Ophthalmologica, 112: 88–91.Google Scholar
Jensen, E. 1966. On the pathology of angiokeratoma corporis diffsum (Fabry). Acta Pathol. Microbiol. Scand., 68: 313–331.CrossRefGoogle Scholar
Kemp, G.L. 1967. Fabry's disease involving the myocardium and coronary arteries. Without skin manifestations. Vase. Dis., 4: 100–106.Google Scholar
Nakao, K., Mizuno, Y., Kano, S., Santo, H., Yano, Y., Mizoguchi, H., Uono, M., Shibata, S., Miyatake, T. 1967. A case of angiokeratoma corporis diffusum (Fabry's disease). [In Japanese]. J. Jap. Soc. Intern. Med., 56: 369–374.Google Scholar
Philippart, M., Franklin, S.S., Gorodon, A. 1972. Reversal of an inborn sphingolipidosis (Fabry's disease) by kidney transplanatation. Ann. Intern. Med., 77: 195–200.Google Scholar
Wise, D. 1960. Angiokeratoma corporis diffusum. Cambridge: Thesis.Google Scholar