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porphyria cutanea tarda
Č. záznamu d017119 Dátum 06.06.2025 Typ M - MESH Tematický termín porphyria cutanea tarda MDT C06.552.830.100C16.320.850.742.250C17.800.827.742.250C18.452.811.400.250 Poznámka 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. 
predmetové heslo
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