Chronische Müdigkeit: Wann liegt der Verdacht auf eine erbliche Stoffwechselerkrankung vor? [Chronic Fatigue: When to Suspect an Inherited Metabolic Disease?]
Détails
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Accès restreint UNIL
Etat: Public
Version: Final published version
Licence: Non spécifiée
Accès restreint UNIL
Etat: Public
Version: Final published version
Licence: Non spécifiée
ID Serval
serval:BIB_37807F248A56
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Chronische Müdigkeit: Wann liegt der Verdacht auf eine erbliche Stoffwechselerkrankung vor? [Chronic Fatigue: When to Suspect an Inherited Metabolic Disease?]
Périodique
Praxis
ISSN
1661-8157 (Print)
ISSN-L
1661-8157
Statut éditorial
Publié
Date de publication
01/2022
Peer-reviewed
Oui
Volume
110
Numéro
1
Pages
1-6
Langue
allemand
Notes
Publication types: Journal Article
Publication Status: ppublish
Publication Status: ppublish
Résumé
Chronic Fatigue: When to Suspect an Inherited Metabolic Disease? Abstract. Chronic fatigue is a non-specific symptom, frequent in outpatient adults' consultations. Persistent physical fatigue of unknown etiology should prompt the search for rare diseases including inherited metabolic disorder (IMD) after elimination of common causes. The main characteristic of chronic fatigue in IMD is its dynamic nature, worsened by circumstances leading to an increased metabolism such as physical exertion, cold, fasting or infection. IMD leading to chronic fatigue are metabolic myopathies, in particular glycogen storage disease affecting muscle, fatty acid oxidation disorders and mitochondrial diseases. The diagnosis is confirmed by specific biochemical and/or molecular analyzes with multidisciplinary management.
Mots-clé
Adult, Fasting, Fatigue Syndrome, Chronic/diagnosis, Fatigue Syndrome, Chronic/etiology, Fatigue Syndrome, Chronic/therapy, Humans, Metabolic Diseases, Muscular Diseases, Rare Diseases, Chronic fatigue, Chronische Müdigkeit, Fatigue chronique, Myopathie, angeborene Stoffwechselstörung, erreur innée du métabolisme, inherited metabolic disorder (IMD), myopathie, myopathy
Pubmed
Création de la notice
24/01/2022 18:36
Dernière modification de la notice
20/08/2024 6:22