TY - CHAP
T1 - Prenatal Diagnosis and Preimplantation Genetic Testing for Inherited Cardiac Diseases
AU - Nannenberg, E. A.
AU - Arens, Y.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Inherited cardiac diseases (cardiomyopathies and channelopathies) are associated with an increased risk of sudden cardiac death (SCD). A common hallmark is the variable disease expression and incomplete penetrance. Therefore the phenotype varies widely between and within families. Carriers of a severe genetic disease have several reproductive options to fulfill their child wish due to progress in molecular genomics and assisted reproductive technology (Prenatal Diagnosis or Preimplantation Genetic Testing (PGT)). In this chapter, we describe the different reproductive techniques and evaluate the number of prenatal diagnoses and referrals for PGT for inherited cardiac diseases in literature and in the Netherlands in the past years. Although inherited cardiac diseases can exhibit a severe phenotype or a severe family history of sudden cardiac death, the number of patients with inherited cardiac diseases opting for and continuing with PND and PGT is small.
AB - Inherited cardiac diseases (cardiomyopathies and channelopathies) are associated with an increased risk of sudden cardiac death (SCD). A common hallmark is the variable disease expression and incomplete penetrance. Therefore the phenotype varies widely between and within families. Carriers of a severe genetic disease have several reproductive options to fulfill their child wish due to progress in molecular genomics and assisted reproductive technology (Prenatal Diagnosis or Preimplantation Genetic Testing (PGT)). In this chapter, we describe the different reproductive techniques and evaluate the number of prenatal diagnoses and referrals for PGT for inherited cardiac diseases in literature and in the Netherlands in the past years. Although inherited cardiac diseases can exhibit a severe phenotype or a severe family history of sudden cardiac death, the number of patients with inherited cardiac diseases opting for and continuing with PND and PGT is small.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85150148084&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/36970708
UR - https://www.ncbi.nlm.nih.gov/pubmed/36911287
U2 - https://doi.org/10.1007/978-3-030-45457-9_27
DO - https://doi.org/10.1007/978-3-030-45457-9_27
M3 - Chapter
C2 - 36970708
SN - 9783030454562
T3 - Clinical Cardiogenetics: Third Edition
SP - 457
EP - 461
BT - Clinical Cardiogenetics: Third Edition
PB - Springer International Publishing
ER -