TY - JOUR
T1 - Apert syndrome
T2 - A case report with discussion of craniofacial features
AU - Paravatty, Rajesh P.
AU - Ahsan, Auswaf
AU - Sebastian, Bastian T.
AU - Pai, Keerthilatha M.
AU - Dayal, Promod K.
PY - 1999/6/1
Y1 - 1999/6/1
N2 - Apert syndrome is a rare congenital anomaly characterized by acrocephaly, syndactyly, and abnormalities of other organs. It has characteristic features in the orofacial region, affecting the eyes, palate, middle third of face, and uvula. In this case report, the features of Apert syndrome, particularly in relation to the orofacial region, are discussed.
AB - Apert syndrome is a rare congenital anomaly characterized by acrocephaly, syndactyly, and abnormalities of other organs. It has characteristic features in the orofacial region, affecting the eyes, palate, middle third of face, and uvula. In this case report, the features of Apert syndrome, particularly in relation to the orofacial region, are discussed.
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M3 - Article
C2 - 10635279
AN - SCOPUS:0033138964
SN - 0033-6572
VL - 30
SP - 423
EP - 426
JO - Quintessence International
JF - Quintessence International
IS - 6
ER -