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A rare cause of sudden unexpected death syndrome (SUDS) in the first year of life: endomyocardial fibroelastosis (EFE) due to two compound heterozygous MYBPC3 mutations.
Hartung, Benno; Tank, Anne; Dittmann, Sven; Ritz-Timme, Stefanie; Schulze-Bahr, Eric.
Affiliation
  • Hartung B; Institute of Legal Medicine, University Hospital Düsseldorf, Moorenstr. 5, 40225, Düsseldorf, Germany. benno.hartung@med.uni-duesseldorf.de.
  • Tank A; Institute of Legal Medicine, University Hospital Düsseldorf, Moorenstr. 5, 40225, Düsseldorf, Germany.
  • Dittmann S; Department of Cardiovascular Medicine, Institute for Genetics of Heart Diseases, University Hospital Münster, 48129, Münster, Germany.
  • Ritz-Timme S; Institute of Legal Medicine, University Hospital Düsseldorf, Moorenstr. 5, 40225, Düsseldorf, Germany.
  • Schulze-Bahr E; Department of Cardiovascular Medicine, Institute for Genetics of Heart Diseases, University Hospital Münster, 48129, Münster, Germany.
BMC Cardiovasc Disord ; 21(1): 174, 2021 04 13.
Article in En | MEDLINE | ID: mdl-33849460
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carrier Proteins / Death, Sudden, Cardiac / Endocardial Fibroelastosis / Mutation Limits: Humans / Infant / Male Language: En Journal: BMC Cardiovasc Disord Journal subject: ANGIOLOGIA / CARDIOLOGIA Year: 2021 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carrier Proteins / Death, Sudden, Cardiac / Endocardial Fibroelastosis / Mutation Limits: Humans / Infant / Male Language: En Journal: BMC Cardiovasc Disord Journal subject: ANGIOLOGIA / CARDIOLOGIA Year: 2021 Document type: Article Affiliation country: Alemania Country of publication: Reino Unido