Albright's hereditary osteodystrophy with extensive heterotopic ossification of the oral and maxillofacial region: how fetuin research may help a seemingly impossible condition

Albright"s hereditary osteodystrophy (AHO) is a complex genetic disorder characterized by brachydactyly, gonadotropin resistance, hypothyroidism, pseudohypoparathyroid syndrome and heterotopic ossification. Heterotopic ossification rarely occurs in the maxillofacial region. In this article, we...

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Veröffentlicht in:Journal (Canadian Dental Association) 2007-11, Vol.73 (9), p.845-850
Hauptverfasser: DuVal, Marc G, Davidson, Sarah, Ho, Andrew, Cohen, Rachale, Park, Michael, Nourian, Somayeh, Baker, Gerald, Sándor, George K B
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Sprache:eng
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Zusammenfassung:Albright"s hereditary osteodystrophy (AHO) is a complex genetic disorder characterized by brachydactyly, gonadotropin resistance, hypothyroidism, pseudohypoparathyroid syndrome and heterotopic ossification. Heterotopic ossification rarely occurs in the maxillofacial region. In this article, we present such a case, describe the etiology, characteristics and treatment of AHO and suggest a potential role of an inhibitor of bone formation such as fetuin in preventing recurrence of aberrant ossification.
ISSN:0709-8936
1488-2159