Nilde-Fornitrici
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[Nilde-fornitrici] capitolo libro
- Subject: [Nilde-fornitrici] capitolo libro
- From: biomedic@uniroma2.it
- Date: Wed, 29 Jul 2026 14:11:49 +0200
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Gentilissime Colleghe e gentilissimi Colleghi,
dopo infruttuose ricerche, mi rivolgo alla Lista per chiedere se
qualcuno di voi accede alla seguente risorsa:
Confidando nella vostra cortese disponibilità, vi auguro buon lavoro.
Ecco i dati del capitolo del libro “Prenatal Diagnosis of Orofacial
Malformations”:
Medina-Hernandez, C., Garcia-Rodriguez, R., Garcia-Delgado, R.,
Martin-Martinez, A., Sepulveda, W. (2025). Solitary Median Maxillary
Central Incisor Syndrome: Prenatal Findings in Three Cases. In: Tonni,
G., Sepulveda, W., Wong, A.E. (eds) Prenatal Diagnosis of Orofacial
Malformations. Springer, Cham.
https://doi.org/10.1007/978-3-031-96947-8_31 (questo il link alla
pagina del sito dell’editore:
https://link.springer.com/chapter/10.1007/978-3-031-96947-8_31#citeas)
Esport dei dati in formato RIS:
TY - CHAP
AU - Medina-Hernandez, Cristina
AU - Garcia-Rodriguez, Raquel
AU - Garcia-Delgado, Raquel
AU - Martin-Martinez, Alicia
AU - Sepulveda, Waldo
ED - Tonni, Gabriele
ED - Sepulveda, Waldo
ED - Wong, Amy E.
PY - 2025
DA - 2025//
TI - Solitary Median Maxillary Central Incisor Syndrome: Prenatal
Findings in Three Cases
BT - Prenatal Diagnosis of Orofacial Malformations
SP - 387
EP - 394
PB - Springer Nature Switzerland
CY - Cham
AB - Technological advances in prenatal diagnostic ultrasound have
led to identifying defects of the midline structures of the head whose
etiology is still largely unknown although mostly related to
underdiagnosed genetic syndromes. We describe three cases of solitary
median maxillary central incisor syndrome in which two-dimensional
second trimester of pregnancy sonography showed the characteristic
dental feature of a solitary central incisor in the maxilla. This
syndrome is a complex condition that may appear isolated or in
association with other midline developmental anomalies within the
broad holoprosencephaly spectrum. Early recognition of the syndrome is
of great importance for establishing the diagnosis, performing
additional investigation, and management of associated anomalies.
SN - 978-3-031-96947-8
UR - https://doi.org/10.1007/978-3-031-96947-8_31
DO - 10.1007/978-3-031-96947-8_31
ID - Medina-Hernandez2025
ER -
Sig. Massimo RICCIUTO
Università degli Studi di Roma Tor Vergata
Collaboratore di Biblioteca
Biblioteca dell’area Biomedica - Paolo M. Fasella
Facoltà di Medicina e Chirurgia
Edificio D, livello 2
Via Montpellier, 1 - 00133 Roma
Telefono: (+39) 06 7259 5420
E-mail: ricciuto@biblio.uniroma2.it
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