Oral and dental abnormalities in Barber–Say syndrome

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...

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Bibliographic Details
Published in:American journal of medical genetics. Part A 2010-10, Vol.152A (10), p.2569-2573
Main Authors: Martins, Fabiana, Ortega, Karem Lopez, Hiraoka, Cybelle, Ricardo, Patricia, Magalhães, Marina
Format: Article
Language:English
Subjects:
Abnormalities, Multiple - genetics
Barber–Say syndrome
Biological and medical sciences
Child, Preschool
Dentition
Dermatology
Diagnosis, Differential
ectropion
Female
Hair and nails disorders
Hirsutism - genetics
Humans
hypertrichosis
macrostomia
Macrostomia - genetics
Male
Medical genetics
Medical sciences
Molar - abnormalities
Molar - diagnostic imaging
Mouth Abnormalities - genetics
Radiography
Syndrome
taurodontism
Tooth Abnormalities - genetics
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Summary: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.
ISSN:1552-4825
1552-4833
1552-4833
DOI:10.1002/ajmg.a.32898