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Albright's hereditary osteodystrophy with extensive heterotopic ossification of the oral and maxillofacial region: how fetuin research may help a seemingly impossible condition.
J Can Dent Assoc 2007; 73(9):845-50JC

Abstract

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.

Authors+Show Affiliations

Mount Sinai Hospital, Toronto, Ontario, Canada.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

18028761

Citation

DuVal, Marc G., et al. "Albright's Hereditary Osteodystrophy With Extensive Heterotopic Ossification of the Oral and Maxillofacial Region: How Fetuin Research May Help a Seemingly Impossible Condition." Journal (Canadian Dental Association), vol. 73, no. 9, 2007, pp. 845-50.
DuVal MG, Davidson S, Ho A, et al. Albright's hereditary osteodystrophy with extensive heterotopic ossification of the oral and maxillofacial region: how fetuin research may help a seemingly impossible condition. J Can Dent Assoc. 2007;73(9):845-50.
DuVal, M. G., Davidson, S., Ho, A., Cohen, R., Park, M., Nourian, S., ... Sándor, G. K. (2007). Albright's hereditary osteodystrophy with extensive heterotopic ossification of the oral and maxillofacial region: how fetuin research may help a seemingly impossible condition. Journal (Canadian Dental Association), 73(9), pp. 845-50.
DuVal MG, et al. Albright's Hereditary Osteodystrophy With Extensive Heterotopic Ossification of the Oral and Maxillofacial Region: How Fetuin Research May Help a Seemingly Impossible Condition. J Can Dent Assoc. 2007;73(9):845-50. PubMed PMID: 18028761.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Albright's hereditary osteodystrophy with extensive heterotopic ossification of the oral and maxillofacial region: how fetuin research may help a seemingly impossible condition. AU - DuVal,Marc G, AU - Davidson,Sarah, AU - Ho,Andrew, AU - Cohen,Rachale, AU - Park,Michael, AU - Nourian,Somayeh, AU - Baker,Gerald, AU - Sándor,George K B, PY - 2007/11/22/pubmed PY - 2007/12/13/medline PY - 2007/11/22/entrez SP - 845 EP - 50 JF - Journal (Canadian Dental Association) JO - J Can Dent Assoc VL - 73 IS - 9 N2 - 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. SN - 1488-2159 UR - https://www.unboundmedicine.com/medline/citation/18028761/Albright's_hereditary_osteodystrophy_with_extensive_heterotopic_ossification_of_the_oral_and_maxillofacial_region:_how_fetuin_research_may_help_a_seemingly_impossible_condition_ L2 - http://www.cda-adc.ca/jcda/vol-73/issue-9/845.html DB - PRIME DP - Unbound Medicine ER -