alexa Balanced Translocation T(6;13)(q21;q34), Multiple Miscarriages, Gingival Fibromatosis - A New Syndrome? | 16786
ISSN: 2247-2452

Oral Health and Dental Management
Open Access

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2nd International Conference and Exhibition on Dental & Oral Health
April 21-23, 2014 Crown Plaza Dubai, UAE

Angel Fenol
ScientificTracks Abstracts: Oral Health Dent Manag
DOI: 10.4172/2247-2452.S1.002
Abstract
Hereditary gingival fibromatosis(HGF) is traditionally considered an autosomal dominant disease, characterized by a slowly progressive, benign enlargement of the keratinized oral gingival tissues that has been mapped to chromosome 2 or chromosome 5. HGF can also be found as a part of various syndromes. This paper highlights a case of hereditary gingival fibromatosis seen in a 11 year old girl. A detailed family history revealed gingival fibromatosis in mother and grandmother. They also had a history of multiple miscarriages. Karyotyping was done and a balanced translocation of chromosome 6 and 13 with break points on 6q21 and 13q34 was found in the child, mother and grandmother. Can this represent an entirely new syndrome?
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