A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Anencephalic infant with cleft palate and natal teeth: A case report
Tekijät: Marakoglu K, Percin EF, Marakoglu I, Gursoy UK, Goze F
Kustantaja: ALLIANCE COMMUNICATIONS GROUP DIVISION ALLEN PRESS
Julkaisuvuosi: 2004
Journal: Cleft Palate Craniofacial Journal
Tietokannassa oleva lehden nimi: CLEFT PALATE-CRANIOFACIAL JOURNAL
Lehden akronyymi: CLEFT PALATE-CRAN J
Vuosikerta: 41
Numero: 4
Aloitussivu: 456
Lopetussivu: 458
Sivujen määrä: 3
ISSN: 1055-6656
DOI: https://doi.org/10.1597/03-024.1
Tiivistelmä
Objective: Natal/neonatal teeth are very common in children with complete unilateral and bilateral cleft lip and palate. This article outlines a patient with intrauterine growth retardation, anencephaly, atrial septal defect, ventricular septal defect, two maxillary first natal incisor teeth, cleft palate, short neck, low-set ears, hypertelorism, retrognathia, and simian-line on the right hand. There is no conclusive evidence of a correlation between these findings and a known syndrome, suggesting that this case may be a hitherto undefined clinical combination with neonatal teeth.
Objective: Natal/neonatal teeth are very common in children with complete unilateral and bilateral cleft lip and palate. This article outlines a patient with intrauterine growth retardation, anencephaly, atrial septal defect, ventricular septal defect, two maxillary first natal incisor teeth, cleft palate, short neck, low-set ears, hypertelorism, retrognathia, and simian-line on the right hand. There is no conclusive evidence of a correlation between these findings and a known syndrome, suggesting that this case may be a hitherto undefined clinical combination with neonatal teeth.
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