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Clinical and biochemical footprints of inherited metabolic disorders: X. Metabolic myopathies

Angelini, Corrado; Burlina, Alberto; Blau, Nenad; Ferreira, Carlos R (2022). Clinical and biochemical footprints of inherited metabolic disorders: X. Metabolic myopathies. Molecular Genetics and Metabolism, 137(1-2):213-222.

Abstract

Metabolic myopathies are characterized by the deficiency or dysfunction of essential metabolites or fuels to generate energy for muscle contraction; they most commonly manifest with neuromuscular symptoms due to impaired muscle development or functioning. We have summarized associations of signs and symptoms in 358 inherited metabolic diseases presenting with myopathies. This represents the tenth of a series of articles attempting to create and maintain a comprehensive list of clinical and metabolic differential diagnoses according to system involvement.

Additional indexing

Item Type:Journal Article, refereed, further contribution
Communities & Collections:04 Faculty of Medicine > University Children's Hospital Zurich > Medical Clinic
Dewey Decimal Classification:610 Medicine & health
Scopus Subject Areas:Health Sciences > Endocrinology, Diabetes and Metabolism
Life Sciences > Biochemistry
Life Sciences > Molecular Biology
Life Sciences > Genetics
Life Sciences > Endocrinology
Uncontrolled Keywords:Endocrinology, Genetics, Molecular Biology, Biochemistry, Endocrinology, Diabetes and Metabolism
Language:English
Date:1 September 2022
Deposited On:28 Feb 2023 10:04
Last Modified:25 Feb 2025 02:39
Publisher:Elsevier
ISSN:1096-7192
OA Status:Closed
Publisher DOI:https://doi.org/10.1016/j.ymgme.2022.09.004
PubMed ID:36155185
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