Empfehlungen

  • Indexpatient mit genetischer Form einer Herzmuskelerkrankung (X
  • Familienangehörige (Verwandte ersten od. höheren Grades) (X)
  • Empfehlungsgrade (X)
Hypertrophe Kardiomyopathie (CMH/HCM)

I42.1/.2  Sarkomer-Erkrankung              
                                                    >25 Unterformen
                                                    Mutation(+) 50-60% 
                                                    Indikation Genetik: I,C
                                                    DiagnoseSelbsthilfe-Gruppe
Arrhythmogene, rechtsventrikuläre Kardiomyopathie (ARVC/ARVD)

I42.80  Desmosomale Erkrankung              
                                                    >10 Unterformen
                                                    Mutation(+) 30-40% 
                                                    Indikation Genetik: I,C
                                                    DiagnoseSelbsthilfe-Gruppe
Linksventrikuläre Non-compaction Kardiomyopathie (LVNC)

I42.9  Sarkomer-Erkrankung              
                                                    >10 Unterformen
                                                    Mutation(+) 20-40% 
                                                    Indikation Genetik: IIa,C
                                                    Diagnose
Dilatative Kardiomyopathie (CMD/DCM)

I42.0  Zytoskelett-Erkrankung              
                                                    >25 Unterformen
                                                    Mutation(+) 15-30% 
                                                    Indikation Genetik: IIa,C
                                                       • DCM+Erregungsleitungsstörung
                                                       • DCM, familiär
                                                    Indikation Genetik: IIb,C
                                                       • DCM, andere
                                                    Diagnose
                                                    Genotypisierung nach
                                                    Rücksprache.
  
Peripartum Kardiomyopathie (PPCM)

I42.0  Sarkomer- bzw. Zytosklelett-Erkrankung (Prädisposition), exogen             
                                                    >10 Unterformen
                                                    Mutation(+) ?! 
                                                    Indikation Genetik: IIb,C
                                                    Diagnose
                                                    Genotypisierung nach
                                                    Rücksprache.
  
Restriktive Kardiomyopathie (RCM)

I42.0  Sarkomer-Erkrankung              
                                                    >2 Unterformen
                                                    Mutation(+) ?! 
                                                    Indikation Genetik: IIb,C
                                                    Diagnose
                                                   
Genotypisierung nach
                                                    Rücksprache.