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Abstract #66388 Published in IGR 17-3
Frank-ter Haar syndrome-additional findings?
Köse TE; İşler C; Şenel ŞN; Şitilci T; Özcan İ; Aksakallı NDento maxillo facial radiology 2016; 45: 20150119
Frank-ter Haar syndrome is a genetic disease that is transmitted by autosomal recessive pattern with characteristic features such as megalocornea or glaucoma, a prominent coccyx, heart defects, developmental delays, brachycephaly, a wide anterior fontanel, finger flexion deformities, full cheeks and micrognathia. Dentomaxillofacial features of this syndrome are not well documented in the literature. We present of a 21-year-old male with Frank-ter Haar syndrome and some features that may be linked with this syndrome not reported before in the literature.
1 Oral and Maxillofacial Radiology Department, Faculty of Dentistry, Istanbul University, Istanbul, Turkey.
Full articleClassification:
9.1.2 Juvenile glaucoma (Part of: 9 Clinical forms of glaucomas > 9.1 Developmental glaucomas)
9.4.15 Glaucoma in relation to systemic disease (Part of: 9 Clinical forms of glaucomas > 9.4 Glaucomas associated with other ocular and systemic disorders)
