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Laterality, heterotaxy, and isolated congenital heart defects : The genetic basis of the segmental nature of the heart.
Putotto, Carolina; Pugnaloni, Flaminia; Unolt, Marta; Calcagni, Giulio; Versacci, Paolo; Marino, Bruno.
Afiliación
  • Putotto C; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, 00161, Italy. carolina.putotto@uniroma1.it.
  • Pugnaloni F; Fetal, Neonatal, and Cardiological Sciences Research Area, Neonatal Intensive Care Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, 00146, Italy.
  • Unolt M; Fetal, Neonatal, and Cardiological Sciences Research Area, Pediatric Cardiology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, 00146, Italy.
  • Calcagni G; Fetal, Neonatal, and Cardiological Sciences Research Area, Pediatric Cardiology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, 00146, Italy.
  • Versacci P; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, 00161, Italy.
  • Marino B; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, 00161, Italy.
Genome Med ; 16(1): 100, 2024 Aug 13.
Article en En | MEDLINE | ID: mdl-39138574
ABSTRACT
To date, the role of NODAL in normal and abnormal L-R asymmetry has been well established. In a recent paper, mutations of this gene have been reported in heterotaxy but also in transposition with D- or L-ventricular loop. The effects of NODAL and other laterality genes can be recognized separately in all three cardiac segments for topology and septation of the atria, for ventricular looping, and for spiralization and alignment of the great arteries.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Heterotaxia / Cardiopatías Congénitas Límite: Animals / Humans Idioma: En Revista: Genome Med Año: 2024 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Heterotaxia / Cardiopatías Congénitas Límite: Animals / Humans Idioma: En Revista: Genome Med Año: 2024 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido