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Oral and dental abnormalities in Barber–Say syndrome
Author(s) -
Martins Fabiana,
Ortega Karem Lopez,
Hiraoka Cybelle,
Ricardo Patricia,
Magalhães Marina
Publication year - 2010
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.32898
Subject(s) - medicine , hypertrichosis , malocclusion , dental anomalies , tooth abnormality , dentistry , hypoplasia , enamel hypoplasia , dermatology , tooth eruption , orthodontics , anatomy , molar , enamel paint
A previously unreported case of Barber–Say syndrome is described with special attention to dental manifestations. A 7‐year‐old female with multiple congenital anomalies such mammary gland hypoplasia, hypertrichosis, ectropion, and redundant skin was seen at the School of Dentistry of the University of São Paulo. Oral examination revealed macrostomia, broad alveolar ridges, gingival fibromatosis, taurodontism, delayed tooth eruption, and malocclusion. Dental treatment included gingivoplasty and orthodontic treatment. © 2010 Wiley‐Liss, Inc.