Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Kerolainy Alves Gadelha"'
Autor:
Bruna Lixinski Diniz, Desirée Deconte, Kerolainy Alves Gadelha, Andressa Barreto Glaeser, Bruna Baierle Guaraná, Andreza Ávila de Moura, Rafael Fabiano Machado Rosa, Paulo Ricardo Gazzola Zen
Publikováno v:
Journal of Pediatric Genetics. 12:113-122
Congenital heart defects (CHDs) are one of the most prevalent clinical features described in individuals diagnosed with 22q11.2 deletion syndrome (22q11.2DS). Therefore, cardiac malformations may be the main finding to refer for syndrome investigatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::579a424709de8831f8db0854679b3b15
https://doi.org/10.1055/s-0043-1763258
https://doi.org/10.1055/s-0043-1763258
Autor:
Gabriel Dotta Abech, Caio Seiti Mestre Okabayashi, Gabriela Rangel Brandão, Paulo Ricardo Gazzola Zen, Rafael Fabiano Machado Rosa, Amanda Thum Welter, Carla Bastos da Costa Almeida, Kerolainy Alves Gadelha
Publikováno v:
J Pediatr Genet
Trisomy 21 is considered the most common chromosomal aneuploidy, and congenital heart disease (CHD) is highly prevalent and relevant to the morbidity and mortality of these patients. Ebstein anomaly (EA) is a rare CHD characterized by tricuspid valve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::379b2dc8add59b0e031596ff07fed631
https://doi.org/10.1055/s-0040-1714360
https://doi.org/10.1055/s-0040-1714360