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.
Odkazy
(8) - ČLÁNKY
(1) - CiBaMed
(1) - KNIHY
predmetové heslo
Počet záznamov: 1
openseadragon
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