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KaRhab: an international online registry for cardiac rhabdomyomas

Cardiac rhabdomyoma (RHM) is considered one of the most frequent benign heart tumors in children. However, encounters with cardiac RHM in clinical practice remain rare. Clinical information is primarily available in the form of single case reports or smaller studies with a shortage of large-scale re...

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Main Authors: Herrmann, Vera-Maria (Author) , Arélin, Maria (Author) , Bergner, Caroline G. (Author) , Herrmann, Julia (Author) , Janz, Paula (Author) , Kiep, Henriette (Author) , Mueller, Annika (Author) , Syrbe, Steffen (Author) , Wagner, Robert (Author) , Wannenmacher, Bardo (Author) , Wolf, Nadine (Author) , Weidenbach, Michael (Author) , Strehlow, Vincent (Author)
Format: Article (Journal)
Language:English
Published: 30 January 2025
In: Orphanet journal of rare diseases
Year: 2025, Volume: 20, Pages: 44-1-44-7
ISSN:1750-1172
DOI:10.1186/s13023-024-03470-w
Online Access:Resolving-System, kostenfrei: https://doi.org/10.1186/s13023-024-03470-w
Resolving-System, kostenfrei: https://doi.org/10.25673/118525
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Author Notes:Vera-Maria Herrmann, Maria Arelin, Caroline G. Bergner, Julia Herrmann, Paula Janz, Henriette Kiep, Annika Mueller, Steffen Syrbe, Robert Wagner, Bardo Wannenmacher, Nadine Wolf, Michael Weidenbach and Vincent Strehlow
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Summary:Cardiac rhabdomyoma (RHM) is considered one of the most frequent benign heart tumors in children. However, encounters with cardiac RHM in clinical practice remain rare. Clinical information is primarily available in the form of single case reports or smaller studies with a shortage of large-scale reviews encompassing a substantial number of cases.
Physical Description:Online Resource
ISSN:1750-1172
DOI:10.1186/s13023-024-03470-w

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