Porphyria Cutanea Tarda [porphyria cutanea tarda]
topical
69
- Terms
-
chronická jaterní porfyrie
porfyrie kožní pozdní
symptomatická jaterní porfyrie
Persistent link
https://www.medvik.cz/link/D017119
Definition
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.
- DUI
- D017119 MeSH Browser
- CUI
- M0026011
- Previous indexing
- Porphyria (1966-1992)
- History note
- 95; was PORPHYRIA, CUTANEA TARDA 1993-94
- Online note
- use PORPHYRIA CUTANEA TARDA to search PORPHYRIA, CUTANEA TARDA 1993-94
- Public note
- 95; was PORPHYRIA, CUTANEA TARDA 1993-94
Allowable subheadings
- BL
- blood 2
- CF
- cerebrospinal fluid
- CI
- chemically induced 2
- CL
- classification 4
- CO
- complications 4
- CN
- congenital
- DI
- diagnosis 23
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 9
- EC
- economics
- EM
- embryology
- EN
- enzymology 1
- EP
- epidemiology 1
- EH
- ethnology
- ET
- etiology 22
- GE
- genetics 5
- HI
- history
- IM
- immunology 2
- ME
- metabolism 2
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 9
- PP
- physiopathology 8
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 11
- UR
- urine 2
- VE
- veterinary
- VI
- virology 3
...
Occurrences in Medvik records
C
Diseases
Porphyria Cutanea Tarda, Type I Disease MeSH Browser