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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| Hauptverfasser: | , , , , , , , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
30 January 2025
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| In: |
Orphanet journal of rare diseases
Year: 2025, Jahrgang: 20, Pages: 44-1-44-7 |
| ISSN: | 1750-1172 |
| DOI: | 10.1186/s13023-024-03470-w |
| Online-Zugang: | Resolving-System, kostenfrei: https://doi.org/10.1186/s13023-024-03470-w Resolving-System, kostenfrei: https://doi.org/10.25673/118525 |
| Verfasserangaben: | 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 |
| Zusammenfassung: | 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. |
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| Beschreibung: | Online Resource |
| ISSN: | 1750-1172 |
| DOI: | 10.1186/s13023-024-03470-w |