<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Meisner JK</submitter><funding>NIDCD NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>81-89</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9451669</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>184(1)</volume><pubmed_abstract>CHARGE syndrome is characterized by a pattern of congenital anomalies (Coloboma of the eye, Heart defects, Atresia of the choanae, Retardation of growth, Genital abnormalities, and Ear abnormalities). De novo mutations of chromodomain helicase DNA binding protein 7 (CHD7) are the primary cause of CHARGE syndrome. The clinical phenotype is highly variable including a wide spectrum of congenital heart defects. Here, we review the range of congenital heart defects and the molecular effects of CHD7 on cardiovascular development that lead to an over-representation of atrioventricular septal, conotruncal, and aortic arch defects in CHARGE syndrome. Further, we review the overlap of cardiovascular and noncardiovascular comorbidities present in CHARGE and their impact on the peri-operative morbidity and mortality in individuals with CHARGE syndrome.</pubmed_abstract><journal>American journal of medical genetics. Part C, Seminars in medical genetics</journal><pubmed_title>Congenital heart defects in CHARGE: The molecular role of CHD7 and effects on cardiac phenotype and clinical outcomes.</pubmed_title><pmcid>PMC9451669</pmcid><funding_grant_id>R01 DC009410</funding_grant_id><funding_grant_id>R01‐014456</funding_grant_id><funding_grant_id>R01-014456</funding_grant_id><pubmed_authors>Martin DM</pubmed_authors><pubmed_authors>Meisner JK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Congenital heart defects in CHARGE: The molecular role of CHD7 and effects on cardiac phenotype and clinical outcomes.</name><description>CHARGE syndrome is characterized by a pattern of congenital anomalies (Coloboma of the eye, Heart defects, Atresia of the choanae, Retardation of growth, Genital abnormalities, and Ear abnormalities). De novo mutations of chromodomain helicase DNA binding protein 7 (CHD7) are the primary cause of CHARGE syndrome. The clinical phenotype is highly variable including a wide spectrum of congenital heart defects. Here, we review the range of congenital heart defects and the molecular effects of CHD7 on cardiovascular development that lead to an over-representation of atrioventricular septal, conotruncal, and aortic arch defects in CHARGE syndrome. Further, we review the overlap of cardiovascular and noncardiovascular comorbidities present in CHARGE and their impact on the peri-operative morbidity and mortality in individuals with CHARGE syndrome.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Mar</publication><modification>2025-05-29T16:11:27.081Z</modification><creation>2025-04-06T01:50:21.601Z</creation></dates><accession>S-EPMC9451669</accession><cross_references><pubmed>31833191</pubmed><doi>10.1002/ajmg.c.31761</doi></cross_references></HashMap>