Very Long Time Persistent HyperCKemia as the First Manifestation of McLeod Syndrome: A Case Report
Mov Disord Clin Pract
.
2022 Jul 3;9(6):821-824.
doi: 10.1002/mdc3.13502.
eCollection 2022 Aug.
Authors
Viviana Torres
1
,
Cèlia Painous
1
,
Pilar Santacruz
1
,
Aurora Sánchez
2
,
Cristina Sanz
3
,
Josep M Grau-Junyent
4
5
6
,
Esteban Muñoz
1
5
6
7
Affiliations
1
Parkinson's Disease and Movement Disorders Unit, Neurology Service, Institut de Neurociencies Hospital Clínic of Barcelona Barcelona Spain.
2
Biochemistry and Molecular Genetics Department Centre de Diagnòstic Biomèdic, Hospital Clínic of Barcelona Barcelona Spain.
3
Blood Bank and Transfusion Service Banc de Sang i Teixits, Hospital Clínic of Barcelona Barcelona Spain.
4
Laboratory of Muscle Research and Mitochondrial Function, Department of Internal Medicine Hospital Clínic of Barcelona Barcelona Spain.
5
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) Barcelona Spain.
6
University of Barcelona Barcelona Spain.
7
European Reference Network-Rare Neurological Diseases (ERN-RND) Barcelona Spain.
PMID:
35937484
PMCID:
PMC9346248
DOI:
10.1002/mdc3.13502
No abstract available
Keywords:
McLeod syndrome; chorea; creatine kinase; neuroacanthocytosis.
Publication types
Case Reports