Aceruloplasminemia: A Severe Neurodegenerative Disorder Deserving an Early Diagnosis.

Aceruloplasminemia iron metabolism iron overload disease neurodegeneration with brain iron accumulation rare anemias

Journal

Frontiers in neuroscience
ISSN: 1662-4548
Titre abrégé: Front Neurosci
Pays: Switzerland
ID NLM: 101478481

Informations de publication

Date de publication:
2019
Historique:
received: 31 10 2018
accepted: 21 03 2019
entrez: 27 4 2019
pubmed: 27 4 2019
medline: 27 4 2019
Statut: epublish

Résumé

Aceruloplasminemia (ACP) is a rare, adult-onset, autosomal recessive disorder, characterized by systemic iron overload due to mutations in the Ceruloplasmin gene (

Identifiants

pubmed: 31024241
doi: 10.3389/fnins.2019.00325
pmc: PMC6460567
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

325

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Auteurs

Giacomo Marchi (G)

Department of Medicine, University of Verona, Verona, Italy.

Fabiana Busti (F)

Department of Medicine, University of Verona, Verona, Italy.

Acaynne Lira Zidanes (A)

Department of Medicine, University of Verona, Verona, Italy.

Annalisa Castagna (A)

Department of Medicine, University of Verona, Verona, Italy.

Domenico Girelli (D)

Department of Medicine, University of Verona, Verona, Italy.

Classifications MeSH