Fatigue chronique: quand suspecter une maladie héréditaire du métabolisme? [Chronic Fatigue: When to Suspect an Inherited Metabolic Disease?]

Details

Serval ID
serval:BIB_8BFFA015F66C
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Fatigue chronique: quand suspecter une maladie héréditaire du métabolisme? [Chronic Fatigue: When to Suspect an Inherited Metabolic Disease?]
Journal
Praxis
Author(s)
Tankeu A.T., Tran C.
ISSN
1661-8157 (Print)
ISSN-L
1661-8157
Publication state
Published
Issued date
01/2022
Peer-reviewed
Oui
Volume
110
Number
1
Pages
38-43
Language
french
Notes
Publication types: Journal Article
Publication Status: ppublish
Abstract
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.
Keywords
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, Inherited Metabolic Disorder (IMD), Myopathie, angeborene Stoffwechselstörung, erreur innée du métabolisme, myopathie, myopathy
Pubmed
Create date
24/01/2022 19:35
Last modification date
28/05/2022 6:35
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