Literature DB >> 18028761

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

Marc G DuVal1, Sarah Davidson, Andrew Ho, Rachale Cohen, Michael Park, Somayeh Nourian, Gerald Baker, George K B Sándor.   

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.

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Year:  2007        PMID: 18028761

Source DB:  PubMed          Journal:  J Can Dent Assoc        ISSN: 0709-8936            Impact factor:   1.316


  2 in total

1.  Prolonged spontaneous normocalcaemia in pseudohypoparathyroidism from resorption of soft tissue calcium deposits: a cautionary tale.

Authors:  Erin E Carter; Gregory Kline
Journal:  BMJ Case Rep       Date:  2014-01-30

2.  Raised intracranial pressure as a result of pansynostosis in a child with Albright's hereditary osteodystrophy.

Authors:  Sepehr Mamoei; Søren Cortnum
Journal:  Childs Nerv Syst       Date:  2016-12-29       Impact factor: 1.475

  2 in total

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