Familial Porphyria Cutanea Tarda.
Rudnick S, Phillips J, Bonkovsky H; Porphyrias Consortium of the Rare Diseases Clinical Research Network.
2013 Jun 6 [updated 2022 Jun 9]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
Porphyria cutanea tarda: Recent update.
Singal AK.
Mol Genet Metab. 2019 Nov;128(3):271-281. doi: 10.1016/j.ymgme.2019.01.004. Epub 2019 Jan 18.
Non-familial porphyria cutanea tarda: a rare disease.
Di Prete M, Ferlosio A, Mazzilli S, Bianchi L, Orlandi A, Campione E.
G Ital Dermatol Venereol. 2020 Oct;155(5):687-688. doi: 10.23736/S0392-0488.18.06052-2. Epub 2018 Sep 18.
Porphyria cutanea tarda.
Bleasel NR, Varigos GA.
Australas J Dermatol. 2000 Nov;41(4):197-206; quiz 207-8. doi: 10.1046/j.1440-0960.2000.00437.x.
Porphyria cutanea tarda.
Elder GH.
Semin Liver Dis. 1998;18(1):67-75. doi: 10.1055/s-2007-1007142.
Hepatoerythropoietic Porphyria.
Rudnick S, Phillips J, Bonkovsky H; Porphyrias Consortium of the Rare Diseases Clinical Research Network.
2013 Oct 31 [updated 2022 Dec 22]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
Familial and sporadic porphyria cutanea tarda: clinical and biochemical features and risk factors in 152 patients.
Muñoz-Santos C, Guilabert A, Moreno N, To-Figueras J, Badenas C, Darwich E, Herrero C.
Medicine (Baltimore). 2010 Mar;89(2):69-74. doi: 10.1097/MD.0b013e3181d50928.
Porphyria cutanea tarda--when skin meets liver.
Frank J, Poblete-Gutiérrez P.
Best Pract Res Clin Gastroenterol. 2010 Oct;24(5):735-45. doi: 10.1016/j.bpg.2010.07.002.
Hepatoerythropoietic porphyria: relationship with familial porphyria cutanea tarda.
Castaño Suárez E, Zamarro Sanz O, Guerra Tapia A, Enríquez de Salamanca R.
Dermatology. 1996;193(4):332-5. doi: 10.1159/000246284.
Porphyria cutanea tarda and hepatoerythropoietic porphyria: Identification of 19 novel uroporphyrinogen III decarboxylase mutations.
Weiss Y, Chen B, Yasuda M, Nazarenko I, Anderson KE, Desnick RJ.
Mol Genet Metab. 2019 Nov;128(3):363-366. doi: 10.1016/j.ymgme.2018.11.013. Epub 2018 Nov 28.
