Pompeova bolest – smjernice za dijagnozu i liječenje odraslih bolesnika [Pompe disease - guidelines for diagnosis and management of adult patients]

Pećin, Ivan and Muačević-Katanec, Diana and Šimić, Iveta and Fumić, Ksenija and Potočki, Kristina and Šućur, Nediljko and Reiner, Željko (2015) Pompeova bolest – smjernice za dijagnozu i liječenje odraslih bolesnika [Pompe disease - guidelines for diagnosis and management of adult patients]. Liječnički vjesnik, 137 (7-8). pp. 216-218. ISSN 0024-3477

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Abstract

These guidelines provide a short summary of recommendations on Pompe disease, how to diagnose this disease, management of adult patients with this disease, follow-up of the patients and recommendations on therapy and genetic testing. Early diagnosis and management of patients with Pompe disease requires a multidisciplinary approach of several different experts. These guidelines were produced by the Division of Metabolic Diseases, Department of Internal Medicine, University Hospital Center Zagreb which is a Referral expert center for rare and metabolic diseases of the Ministry of Health of the Republic of Croatia. They were endorsed by the Croatian Society for Rare Diseases, Croatian Medical Association.These are the first guidelines published in Croatia on diagnosis, treatment and follow-up of Pompe disease.

Abstract in Croatian

Ove smjernice daju kratke naputke o Pompeovoj bolesti: kako dijagnosticirati, liječiti i pratiti bolesnike koji boluju od ove rijetke lizosomske bolesti nakupljanja. Rano postavljanje dijagnoze i liječenje bolesnika s Pompeovom bolesti zahtijevaju multidisciplinarni pristup niza stručnjaka. Smjernice su sastavili stručnjaci koji imaju iskustvo u radu s bolesnicima oboljelima od rijetkih bolesti metabolizma i plod su iskustva rada s rijetkim bolestima u Zavodu za bolesti metabolizma Klinike za unutarnje bolesti, KBC Zagreb, Referentnog centra Ministarstva zdravlja i socijalne skrbi Republike Hrvatske za rijetke i metaboličke bolesti. Smjernice su prihvaćene na Godišnjoj skupštini Hrvatskog društva za rijetke bolesti Hrvatskoga liječničkog zbora. Radi se o prvim takvim smjernicama u Republici Hrvatskoj pa se ovom inicijativom (uz smjernice o Gaucherovoj i Fabryjevoj bolesti) Hrvatska priključuje ostalim europskim državama koje su donijele smjernice iz područja rijetkih bolesti metabolizma.

Item Type: Article
MeSH: Adult ; Croatia ; Enzyme Replacement Therapy ; Genetic Testing ; Glucan 1,4-alpha-Glucosidase/therapeutic use ; Glycogen Storage Disease Type II/diagnosis ; Glycogen Storage Disease Type II/genetics ; Glycogen Storage Disease Type II/therapy ; Humans
Departments: Katedra za internu medicinu
Katedra za radiologiju i opću kliničku onkologiju
Depositing User: Anja Majstorović
Status: Published
Creators:
CreatorsEmail
Pećin, IvanUNSPECIFIED
Muačević-Katanec, DianaUNSPECIFIED
Šimić, IvetaUNSPECIFIED
Fumić, KsenijaUNSPECIFIED
Potočki, KristinaUNSPECIFIED
Šućur, NediljkoUNSPECIFIED
Reiner, ŽeljkoUNSPECIFIED
Date: July 2015
Date Deposited: 15 Mar 2019 10:54
Last Modified: 23 Jul 2020 09:23
Subjects: /
Related URLs:
URI: http://medlib.mef.hr/id/eprint/3119

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