Results 161 to 170 of about 1,705 (212)
Screening for acute hepatic porphyria in postural tachycardia syndrome. [PDF]
Clin Auton ResMwesigwa N +7 more
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Understanding Coproporphyrins and Their Disposition: Coproporphyrinuria is Common, of Diverse Cause, and Rarely Indicates Porphyria. [PDF]
Am J MedBonkovsky HL +5 more
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Porphyria Cutanea Tarda: A Multifactorial Disease. [PDF]
CureusBaltazar AM, Savka L, Carreira NR.
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Seminars in Liver Disease, 1998
Variegate porphyria is an autosomal dominant inherited trait resulting in decreased activity of protoporphyrinogen oxidase. It is characterized clinically by photosensitive skin disease and a propensity to acute neurovisceral crises. The disease is found worldwide but has an exceptionally high frequency in South Africa.
R E, Kirsch, P N, Meissner, R J, Hift
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Variegate porphyria is an autosomal dominant inherited trait resulting in decreased activity of protoporphyrinogen oxidase. It is characterized clinically by photosensitive skin disease and a propensity to acute neurovisceral crises. The disease is found worldwide but has an exceptionally high frequency in South Africa.
R E, Kirsch, P N, Meissner, R J, Hift
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Coexistent Variegate Porphyria and Porphyria Cutanea Tarda
New England Journal of Medicine, 1982VARIEGATE porphyria is inherited as an autosomal dominant disorder with the clinical characteristics of cutaneous involvement and acute attacks, although these features do not always accompany one ...
R S, Day, L, Eales, D, Meissner
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Variegate Porphyria in New England
JAMA: The Journal of the American Medical Association, 1982Variegate porphyria (VP) is an autosomal dominant disease characterized in adults by mechanical fragility and blistering of sun-exposed skin or acute visceral and neurological manifestations. The laboratory diagnosis of VP depends on a search for high levels of coproporphyrin and protoporphyrin in the feces.
J E, Muhlbauer +3 more
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The Journal of Dermatology, 2004
AbstractVariegate porphyria is a rare, hereditary form of hepatic porphyria characterized by acute systemic symptoms as in acute intermittent porphyria in addition to cutaneous symptoms simulating porphyria cutanea tarda. We describe a 22‐year‐old female from India who first presented to the emergency department with acute symptoms and was later ...
Kamaldeep, Sandhu, Bhushan, Kumar
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AbstractVariegate porphyria is a rare, hereditary form of hepatic porphyria characterized by acute systemic symptoms as in acute intermittent porphyria in addition to cutaneous symptoms simulating porphyria cutanea tarda. We describe a 22‐year‐old female from India who first presented to the emergency department with acute symptoms and was later ...
Kamaldeep, Sandhu, Bhushan, Kumar
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Annals of Internal Medicine, 1978
In temperate and cold climates the most usual presenting symptom of variegate porphyria is an acute porphyric attack, indistinguishable from that seen in acute intermittent porphyria. Increased fragility of the skin in sun-exposed areas occurs in only half of such patients, and even then is usually mild and easily overlooked.
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In temperate and cold climates the most usual presenting symptom of variegate porphyria is an acute porphyric attack, indistinguishable from that seen in acute intermittent porphyria. Increased fragility of the skin in sun-exposed areas occurs in only half of such patients, and even then is usually mild and easily overlooked.
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Late onset variegate porphyria
Clinical and Experimental Dermatology, 1996Variegate porphyria (VP) first presenting in old age is uncommon and should raise the possibility of an underlying precipitating cause. This case report documents VP in an elderly woman with a liver tumour.
S A, Grabczynska +2 more
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