Czech Society of Hepatology guidelines for diagnosis and treatment of acute porphyrias

Česká verzia

Authors: R. Brůha ¹; L. Vítek ^1,2; J. Šperl ³ ; P. Urbánek ⁴
Authors place of work: IV. interní klinika – klinika gastroenterologie a hepatologie 1. LF UK a VFN v Praze ¹; Ústav lékařské biochemie a laboratorní diagnostiky, 1. LF UK a VFN v Praze ²; Klinika hepatogastroenterologie, Transplantcentrum, IKEM, Praha ³; Interní klinika 1. LF UK a ÚVN Praha ⁴
Published in the journal: Gastroent Hepatol 2017; 71(2): 101-104
Category: Hepatologie: doporučené postupy
doi: https://doi.org/10.14735/amgh2017101

Porfyrie jsou vzácné metabolické choroby způsobené vrozeným enzymatickým defektem nebo získanou poruchou syntézy hemu. Důsledkem enzymatického defektu je zvýšená tvorba porfyrinů, porfyrinogenů či jejich prekurzorů vedoucí k jejich hromadění ve tkáních, případně ke zvýšenému vylučování do moči a stolice.

Summary

The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study.

The Editorial Board declares that the manuscript met the ICMJE „uniform requirements“ for biomedical papers.

Submitted:
7. 3. 2017

Accepted:
20. 3. 2017

Zdroje

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