Results 31 to 40 of about 4,513 (197)

A rare case of porphyria cutanea tarda in a patient with a homozygous hereditary hemochromatosis gene H63D mutation in the setting of hereditary hemochromatosis [PDF]

JAAD Case Reports
Jonathan Banta, MD, Joshua Collins, DO, Todd Kobayashi, MD   +2 more
doaj   +2 more sources

Persistent Beetroot Colored Urine in a Three-Year-Old Child: A Case Report. [PDF]

Clin Case Rep
Clinically manifest porphyria cutanea tarda (PCT) is rare in children. Of ~1400 cases diagnosed at Porphyria Center Sweden, only five were children, all with pathogenic UROD variants and HFE homozygous. Diagnosis is often delayed; in our case, beetroot‐red urine prompted suspicion despite the absence of cutaneous symptoms.
Harper P, Törnhage CJ, Sardh E.
europepmc   +2 more sources

Urinary porphyrin excretion in hepatitis C infection [PDF]

, 1999
A high prevalence of hepatitis C virus infection in porphyria cutanea tarda in some populations suggests a close link between viral hepatitis and alteration of porphyrin metabolism.
Jacob, Karl, Vogeser, Michael, Zachoval, Reinhart   +2 more
core   +1 more source

Porphyrias associated with malignant tumors: Results of treatment with ionizing irradiation [PDF]

, 2001
Background: Porphyrin metabolism disorders, known as porphyria, represent inherited or acquired diseases. The development of porphyria due to light sensibility occurs especially with exposure to wavelengths in the range of 300-700 nm.
Dühmke, Eckhart, Panzer, M., Schaffer, Moshe, Schaffer, Pamela Manuela, Wilkowski, R.   +4 more
core   +1 more source

Porphyria Cutanea Tarda [PDF]

Mayo Clinic Proceedings, 2021
Mauricio F. Jin, Carilyn N. Wieland
openaire   +5 more sources

Human immunodeficiency virus associated sporadic nonfamilial porphyria cutanea tarda

Indian 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, Debabrata Bandyopadhyay, Abanti Saha, Niharika Ranjan Lal   +3 more
doaj   +1 more source

Acute Hepatic Porphyrias: Review and Recent Progress. [PDF]

, 2019
The acute hepatic porphyrias (AHPs) are a group of four inherited diseases of heme biosynthesis that present with episodic, acute neurovisceral symptoms.
Andant, Anderson, Andersson, Badawy, Balwani, Bissell, Bissell, Bloomer, Bonkovsky, Bonkovsky, Bonkovsky, Bonkovsky, Bonkowsky, Bonkowsky, Bonkowsky, Bylesjo, Chen, D’Avola, Ferrer, Glueck, Handschin, Jeans, Lambrecht, Lane, Marsden, McGuire, Pallet, Sardh, Sardh, Shen, Singal, Stein, Stewart, Tchernitchko, Wahlin, Watson, Watson, Willandt, Wu, Yarra, Yasuda   +40 more
core   +1 more source

Porphyria cutanea tarda: A novel mutation

Pediatric 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, Bhavna Dhingra, Dinesh Asati, Garima Goel, Ujjawal Khurana, Girish Chandra Bhatt   +5 more
doaj   +1 more source

Sun, alcohol, and skin lesions

Emergency Care Journal, 2023
A 65-year-old man presented to the emergency room with blistered not itching skin lesions on the dorsal surface of both hands, which developed recurrently after exposure to sun and solved spontaneously with scarring.
Erika Poggiali, Andrea Vercelli
doaj   +1 more source

C-hepatiidi viirusega seotud ekstrahepaatilised [PDF]

, 2007
C-hepatiidi viirus, põhjustades ägedat või kroonilist hepatiiti ning maksatsirroosi, võib olla patogeneetiline tegur ka mitmete teiste kliiniliste ilmingute kujunemisel.
Salupere, Riina
core   +2 more sources