Number of the records: 1  

porphyria cutanea tarda

  1. Record numberd017119
    Date06.06.2025
    TypeM - MESH
    Topical termporphyria cutanea tarda
    UDCC06.552.830.100C16.320.850.742.250C17.800.827.742.250C18.452.811.400.250
    NoteAn 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.
    subject heading

    subject heading

Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.

Accept allSettingsReject all