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Clinical Observation, Diagnostics, and Therapy for Symptomatic and Hereditary Porphyria Cutanea Tarda

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Diagnosis and Therapy of Porphyrias and Lead Intoxication

Abstract

In our experience, porphyria cutanea tarda (PCT) is the most frequently encountered porphyrinopathy in Italy. In the last 9 years, at our institute’s center for porphyrinopathy study, we have observed 203 cases of apparently symptomatic PCT and 18 cases of hereditary PCT, whereas all the other porphyrias (acute intermittent porphyria, porphyria variegata, erythropoietic protoporphyria, Giinther’s disease, hereditary erythropoietic coproporphyria) did not add up to 40 cases.

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References

  1. Topi, G.C., D’Alessandro Gandolfo, L.: Aspetti matabolici ed alterazioni biochimiche della porfiria cutanea tardiva. Boll. 1st. Dermatol. S. Gallicano 7 93–112 (1971)

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  2. Topi, G.C., D’Alessandro Gandolfo, L. : Liver in Porphyria cutanea tarda. In: Porphyrins in Human Diseases. Doss, M. (ed.). Basel: Karger 1976, pp. 312–324

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© 1978 Springer-Verlag Berlin Heidelberg

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Topi, G.C., Gandolfo, L.D. (1978). Clinical Observation, Diagnostics, and Therapy for Symptomatic and Hereditary Porphyria Cutanea Tarda. In: Doss, M. (eds) Diagnosis and Therapy of Porphyrias and Lead Intoxication. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-67002-2_16

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  • DOI: https://doi.org/10.1007/978-3-642-67002-2_16

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-08863-9

  • Online ISBN: 978-3-642-67002-2

  • eBook Packages: Springer Book Archive

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