| Naslov: | Diagnostic delay in inherited metabolic diseases : insights from the U-IMD registry |
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| Avtorji: | ID Teinert, Julian (Avtor)
ID Gleich, Florian (Avtor)
ID Kožich, Viktor (Avtor)
ID Dionisi-Vici, Carlo (Avtor)
ID Bellusci, Marcello (Avtor)
ID Haas, Dorothea (Avtor)
ID Ješina, Pavel (Avtor)
ID Martinelli, Diego (Avtor)
ID Pérez-Mohand, Patricia (Avtor)
ID Burlina, Alberto (Avtor)
ID Grošelj, Urh (Sodelavec pri raziskavi), et al. |
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| Datoteke: |  PDF - Predstavitvena datoteka, prenos (886,47 KB)
MD5: 81F5CC250839D107834F54CF68A1813D
 URL - Izvorni URL, za dostop obiščite https://www.gimjournal.org/article/S1098-3600(26)00872-5/fulltext
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| Jezik: | Angleški jezik |
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| Tipologija: | 1.01 - Izvirni znanstveni članek |
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| Organizacija: |  UKC LJ - Univerzitetni klinični center Ljubljana
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| Povzetek: | Purpose: Early diagnosis and timely initiation of treatment have been shown to be crucial to improve clinical outcomes in individuals with inherited metabolic diseases (IMDs). However, comprehensive data on the diagnostic process and the potential diagnostic delay in IMDs are scarce. This study aims to systematically investigate the diagnostic process in IMDs. Methods: Data were obtained from the Unified European registry for Inherited Metabolic Diseases (U-IMD), the patient registry of the European Reference Network MetabERN. Results: Data were available for 3747 individuals with confirmed diagnosis of one of 345 IMDs. Median age at symptom onset was 120 days. The majority of participants were diagnosed after presenting with symptoms, median diagnostic delay in this group was 270 days, with 47.6% experiencing a diagnostic delay of at least one year. Diagnostic delay did not seem to have changed substantially within the last two decades in this cohort; however, it varied greatly among single IMDs and different IMD disease groups. Conclusion: Diagnostic delay and concomitantly delayed start of specific therapies is a significant risk of poor outcome for individuals with IMDs, highlighting the urgent need to expand newborn screening programs and to establish (ultra-)rapid genome sequencing in critically ill children. |
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| Ključne besede: | European Reference Network for Hereditary Metabolic Disorders, MetabERN, U-IMD, Unified European Registry for Inherited Metabolic Disorders, diagnostic odyssey, inherited metabolic diseases |
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| Status publikacije: | Objavljeno |
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| Verzija publikacije: | Objavljena publikacija |
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| Leto izida: | 2026 |
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| Št. strani: | str. 1-10 |
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| Številčenje: | Vol. 28, issue 5, [article no.] 102554 |
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| PID: | 20.500.12556/DiRROS-29186  |
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| UDK: | 616-053.2 |
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| ISSN pri članku: | 1530-0366 |
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| DOI: | 10.1016/j.gim.2026.102554 |
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| COBISS.SI-ID: | 274665475 |
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| Opomba: | Nasl. z nasl. zaslona;
Opis z dne 9. 4. 2026;
Sodelavec pri raziskavi iz Slovenije: Urh Grošelj;
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| Datum objave v DiRROS: | 23.04.2026 |
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| Število ogledov: | 78 |
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| Število prenosov: | 55 |
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| Metapodatki: |    |
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