Results 21 to 30 of about 1,932 (163)

Early diagnosis of porphyria cutanea tarda as a key to avoiding scarring – a mild form of the disease

open access: yesPrzegląd Dermatologiczny, 2019
Porphyria cutanea tarda belongs to the group of porphyrias. Porphyria is a heme disorder caused by an acquired or congenital defect of hepatic enzymes. This consequently leads to the accumulation of porphyrins in various organs.
Marcela Nowak   +3 more
doaj   +1 more source

Porphyria Cutanea Tarda Presenting as Erythema-multiforme Like Lesions

open access: yesJournal of Nepal Health Research Council, 2019
Porphyria cutaneatarda, is the most common type of porphyria.It is characterized by defective uroporphyrinogen III decarboxylase enzyme.It presents with erosion, bulla with milia formation and sometimes with hypertrichosis and abnormal pigmentation ...
Niraj Parajuli   +2 more
doaj   +1 more source

HAART: a risk factor for development of porphyria cutanea tarda?

open access: yesRevista da Sociedade Brasileira de Medicina Tropical, 2012
Porphyria cutanea tarda (PCT) is caused by inherited or acquired partial deficiency of the uroporphyrinogen-decarboxylase (Uro-D) enzyme activity. It is the most common form of porphyria.
Fred Bernardes Filho   +7 more
doaj   +1 more source

Allogeneic corneoscleral limbus tissue transplantation for treatment of the necrosis in porphyria eye disease [PDF]

open access: yesInternational Journal of Ophthalmology, 2014
Porphyria cutanea tarda (PCT) with ocular complications are rarely reported. To the best of our knowledge, no reports exist on allogeneic corneoscleral limbus tissue transplantation for treatment of these. Amniotic membrane grafting had been performed in
Feng Yan   +4 more
doaj   +1 more source

Scleral Necrosis in Porphyria Cutanea Tarda: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2022
Scleral necrosis is a rare but well documented ocular manifestation of Porphyria Cutanea Tarda (PCT). The PCT is caused by a deficiency of Uroporphyrinogen Decarboxylase (Uro-D).
Ruchi Shukla   +2 more
doaj   +1 more source

An overview of the cutaneous porphyrias [version 1; referees: 2 approved]

open access: yesF1000Research, 2017
This is an overview of the cutaneous porphyrias. It is a narrative review based on the published literature and my personal experience; it is not based on a formal systematic search of the literature.
Robert Dawe
doaj   +1 more source

Unusual case of corneo-scleral melt treated with scleral patch graft in a patient of Porphyria Cutanea Tarda

open access: yesIndian Journal of Ophthalmology. Case Reports, 2021
Porphyria cutanea tarda (PCT) is the most common form of Porphyria, which is a group of metabolic disorders of haem biosynthesis characterized by the involvement of the skin, eyes, and neuro-visceral tissue.
Sweety G Tiple   +3 more
doaj   +1 more source

Porfiria cutânea tardia Porphyria cutanea tarda

open access: yesAnais Brasileiros de Dermatologia, 2006
Trata-se de revisão sobre a porfiria cutânea tardia em que são abordados a fisiopatogenia, as características clínicas, as doenças associadas, os fatores desencadeantes, a bioquímica, a histopatologia, a microscopia eletrônica, a microscopia de ...
Fátima Mendonça Jorge Vieira   +1 more
doaj   +1 more source

Human immunodeficiency virus associated sporadic nonfamilial porphyria cutanea tarda

open access: yesIndian Journal of Dermatology, 2016
Porphyria cutanea tarda (PCT), a relatively uncommon metabolic disease, is the most common cutaneous porphyria. Here, we present the case of a patient diagnosed with sporadic, nonfamilial PCT that presented with classical cutaneous findings and multiple ...
Sibashish Kamal Guha   +3 more
doaj   +1 more source

Porphyria cutanea tarda: A novel mutation

open access: yesPediatric Hematology Oncology Journal, 2016
A 5 year old child with waxing and waning vesicobullous lesions on exposed parts since two years. Blood porphyrin levels were increased and Woods lamp revealed erythrodontia. DNA analysis showed the child was homozygous and both parents were heterozygous
Rajesh Patil   +5 more
doaj   +1 more source

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