Begreppsinformation
Föredragen term
Porphyria Cutanea Tarda
Typ
-
Topical Descriptor
Överordnat begrepp
Användningsanmärkning
- An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form.
Anmärkning om ändringshistoria
- 95; was PORPHYRIA, CUTANEA TARDA 1993-94
Termer på andra språk
-
finska
-
hidas ihoporfyria
-
hidas porfyria
-
ihoporfyria
-
krooninen ihoporfyria
-
porphyria cutanea tarda
-
svenska
URI
http://www.yso.fi/onto/mesh/D017119
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