Results 71 to 80 of about 4,513 (197)
Practical recommendations for biochemical and genetic diagnosis of the porphyrias
Liver International, Volume 45, Issue 3, March 2025.Abstract The porphyrias are a group of rare inborn errors of metabolism associated with various clinical presentations and long‐term complications, making them relevant differential diagnoses to consider for many clinical specialities, especially hepatologists, gastroenterologists and dermatologists.
Aasne K. Aarsand +4 more
wiley +1 more source
Archives of dermatology, 1968 A case of porphyria cutanea tarda is presented in which clinical and biochemical remission were associated with the administration of 0.5 gm of chloroquine twice weekly over a seven-month period without adverse effects.
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Hereditary Hemochromatosis Unmasked by Yersiniosis: Report of Three Cases
Clinical Case Reports, Volume 13, Issue 1, January 2025.ABSTRACT Yersiniosis has a causal relationship with hereditary hemochromatosis (HH). Physicians should have a high index of suspicion for the diagnosis of HH when approaching a patient with yersiniosis in the setting of high ferritin levels and increased iron saturation. Yersiniosis serves as a precursor for the diagnosis of HH.
Karam Karam, Elias Fiani
wiley +1 more source
Direct-acting antivirals for hepatitis C virus induce a rapid clinical and biochemical remission of porphyria cutanea tarda [PDF]
, 2020 Sporadic porphyria cutanea tarda (PCT) is strongly associated with hepatitis C virus (HCV) infection in our population. 1-4 Therapeutic options for PCT include phlebotomies and low-dose 4-aminoquinolines, which show high rates of disease remission ...
Aguilera, Paula +4 more
core +1 more source
Erythropoietic protoporphyrias: Pathogenesis, diagnosis and management
Liver International, Volume 45, Issue 1, January 2025.Abstract The erythropoietic protoporphyrias consist of three ultra‐rare genetic disorders of the erythroid heme biosynthesis, including erythropoietic protoporphyria (EPP1), X‐linked protoporphyria (XLEPP) and CLPX‐protoporphyria (EPP2), which all lead to the accumulation of protoporphyrin IX (PPIX) in erythrocytes.
Anna‐Elisabeth Minder +4 more
wiley +1 more source
Pregnancy Induced Porphyria Cutanea Tarda
Indian Journal of Dermatology, 2000 Prophyria cutanea tarda induced by pregnancy in a 20 year old primi is described along with clinical, biochemical and histological features. All the lesions expect hypertrichosis resolved following childbirth.
Shanker B +4 more
doaj
Miscellanea. Könyvismertetés [PDF]
, 2015 Könyvismertetés. J. R.Nunley, E. V. Lerma (Eds.): Dermatological manifestations of kidney disease Springer-Verlag New York, 2015 267 oldal ISBN 978-1-4939-2394-
Schneider, Imre
core +1 more source
JEADV Clinical Practice, Volume 3, Issue 5, Page 1570-1575, December 2024.Abstract Background The field of artificial intelligence is rapidly evolving. As an easily accessible platform with vast user engagement, the Chat Generative Pre‐Trained Transformer (ChatGPT) holds great promise in medicine, with the latest version, GPT‐4, capable of analyzing clinical images.
Jacob P. S. Nielsen +3 more
wiley +1 more source
International Wound Journal, Volume 21, Issue 12, December 2024.Abstract Toxic epidermal necrolysis (TEN) is a severe skin reaction caused by extensive epidermal and mucosal necrosis. This clinical phenomenon is known as an acute syndrome of apoptotic pan‐epidermolysis (ASAP). The ASAP phenomenon is observed in conditions that mimic TEN, highlighting the challenge in distinguishing these conditions.
Bahareh Abtahi‐Naeini +3 more
wiley +1 more source
Photosensitivity Skin Disorders in Childhood [PDF]
, 2010 Photosensitivity in childhood is caused by a diverse group of diseases. A specific sensitivity of a child’s skin to ultraviolet light is often the first manifestation or a clinical symptom of photodermatosis.
Ines Sjerobabski-Masnec +4 more
core +1 more source