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Porphyria cutanea tarda. Diagnosis, management, and differentiation from other hepatic porphyrias.
Dermatol Clin. 1986 Apr; 4(2):297-309.DC

Abstract

Porphyria cutanea tarda is a photocutaneous syndrome characterized clinically by cutaneous fragility, bullae, hypertrichosis, pigmentary changes, and sclerodermoid plaques and characterized biochemically by hepatic overproduction and storage of excessive amounts of porphyrins. Porphyria cutanea tarda, the most common disorder of porphyrin metabolism, must be differentiated from variegate porphyria, hereditary coproporphyria, bullous dermatosis of hemodialysis, and drug-related pseudoporphyria.

Authors

No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

3955900

Citation

Grossman, M E., and M B. Poh-Fitzpatrick. "Porphyria Cutanea Tarda. Diagnosis, Management, and Differentiation From Other Hepatic Porphyrias." Dermatologic Clinics, vol. 4, no. 2, 1986, pp. 297-309.
Grossman ME, Poh-Fitzpatrick MB. Porphyria cutanea tarda. Diagnosis, management, and differentiation from other hepatic porphyrias. Dermatol Clin. 1986;4(2):297-309.
Grossman, M. E., & Poh-Fitzpatrick, M. B. (1986). Porphyria cutanea tarda. Diagnosis, management, and differentiation from other hepatic porphyrias. Dermatologic Clinics, 4(2), 297-309.
Grossman ME, Poh-Fitzpatrick MB. Porphyria Cutanea Tarda. Diagnosis, Management, and Differentiation From Other Hepatic Porphyrias. Dermatol Clin. 1986;4(2):297-309. PubMed PMID: 3955900.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Porphyria cutanea tarda. Diagnosis, management, and differentiation from other hepatic porphyrias. AU - Grossman,M E, AU - Poh-Fitzpatrick,M B, PY - 1986/4/1/pubmed PY - 1986/4/1/medline PY - 1986/4/1/entrez SP - 297 EP - 309 JF - Dermatologic clinics JO - Dermatol Clin VL - 4 IS - 2 N2 - Porphyria cutanea tarda is a photocutaneous syndrome characterized clinically by cutaneous fragility, bullae, hypertrichosis, pigmentary changes, and sclerodermoid plaques and characterized biochemically by hepatic overproduction and storage of excessive amounts of porphyrins. Porphyria cutanea tarda, the most common disorder of porphyrin metabolism, must be differentiated from variegate porphyria, hereditary coproporphyria, bullous dermatosis of hemodialysis, and drug-related pseudoporphyria. SN - 0733-8635 UR - https://www.unboundmedicine.com/medline/citation/3955900/Porphyria_cutanea_tarda__Diagnosis_management_and_differentiation_from_other_hepatic_porphyrias_ L2 - http://www.diseaseinfosearch.org/result/5879 DB - PRIME DP - Unbound Medicine ER -