Articolul precedent |
Articolul urmator |
476 32 |
Ultima descărcare din IBN: 2024-04-05 05:15 |
SM ISO690:2012 PITEL, Diana. Porfiria hepatică acută – accente pe diagnostic și tratament. In: Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”, 21-23 octombrie 2020, Chişinău. Chişinău: USMF, 2020, p. 247. |
EXPORT metadate: Google Scholar Crossref CERIF DataCite Dublin Core |
Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină şi Farmacie „Nicolae Testemiţanu” 2020 | ||||||
Congresul "Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”" Chişinău, Moldova, 21-23 octombrie 2020 | ||||||
|
||||||
Pag. 247-247 | ||||||
|
||||||
Descarcă PDF | ||||||
Rezumat | ||||||
Background. Porphyria are inherited or acquired diseases due to defects in specific enzymes in the heme biosynthesis process. Depending on the initial site of overproduction and accumulation of porphyrin precursors, they are classified as hepatic porphyria and erythropoietic porphyry. Objective of the study. updating of evolution, clinical information and treatment criteria in acute hepatic porphyria Material and Methods. Analysis of clinical and theoretical research in the last 5 years, on the diagnosis and modern treatment in acute hepatic porphyria Results. The acute hepatic porphyrias (AHPs) are a group of four inherited diseases of heme biosynthesis that present with episodic, acute neurovisceral symptoms. Symptomatic attacks occur primarily in females between 14 and 45 years of age. Their diagnoses are often missed or delayed because the clinical symptoms mimic other more common disorders. There are no reported cases of acute hepatic porphyria in the Republic of Moldova. As well there are not standards and national protocols of behavior for patients. Conclusion. Hepatic porphyria is a rare pathology, without specific clinical manifestations, to establish the diagnosis we need a degree of clinical suspicion and a laboratory where metabolic dosages of porphyrins are possible. |
||||||
Cuvinte-cheie Hepatic porphyria porphirin porphobilinogen, porfirie hepatică porfirine porfobilinogen |
||||||
|