Hereditary uroporphyrinogen-decarboxylase deficiency predisposing porphyria cutanea tarda (chronic hepatic porphyria) in females after oral contraceptive medication-Reference-Cited by-同舟云学术

Hereditary uroporphyrinogen-decarboxylase deficiency predisposing porphyria cutanea tarda (chronic hepatic porphyria) in females after oral contraceptive medication

Published:1985-10 Issue:1 Volume:278 Page:13-16
ISSN:0340-3696
Container-title:Archives of Dermatological Research
language:en
Short-container-title:Arch Dermatol Res

Author:

Sixel-Dietrich F.,Doss M.

Publisher

Springer Science and Business Media LLC

Subject

Dermatology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF00412489.pdf

Reference34 articles.

1. Anderson KE, Bradlow HL, Sassa S, Kappas A (1979) Studies in porphyria. VII. Relationship of the 5?-reductive metabolism of steroid hormones to clinical expression of the genetic defect in acute intermittent porphyria. Am J Med 66:644?650

2. Becker FT (1965) Porphyria cutanea tarda induced by estrogens. Arch Dermatol 92:252?255

3. Benedetto AV, Kushner JP, Taylor JS (1978) Porphyria cutanea tarda in three generations of a single family. N Engl J Med 298:358?362

4. de Salamanca RE, Mingo D, Chinarro S, Munoz JJ, Perpin� J (1982) Patterns of porphyrin excretion in female estrogeninduced porphyria cutanea tarda. Arch Dermatol Res 274:179?184.

5. de Verneuil H, Aitken G, Nordmann Y (1978) Familial and sporadic porphyria cutanea. Two different diseases. Hum Genet 42:145?151

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