Literature DB >> 10457258

Polycystic bone disease: A new, autosomal dominant disorder.

M P Whyte1, M C Eddy, M N Podgornik, W H McAlister.   

Abstract

We describe a new heritable bone disease characterized radiographically by increasingly numerous and enlarging cyst-like lesions throughout the skeleton. Beginning in early childhood, a father, son, and daughter all suffered from progressively frequent pathological fractures involving such radiolucencies. Healing occurred uneventfully and with little residual pain or deformity. Biochemical parameters of mineral homeostasis and skeletal turnover were normal. Bone scanning showed increased radioisotope uptake primarily in fractures and in the largest collections of the lesions. The histopathology is uncertain, but may reflect a form of intraosseous lipomatosis. This unique condition, which we have provisionally named polycystic bone disease, is inherited as an autosomal dominant trait with a high degree of penetrance.

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Year:  1999        PMID: 10457258     DOI: 10.1359/jbmr.1999.14.8.1261

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN: 0884-0431            Impact factor:   6.741


  2 in total

1.  Multiple Intraosseous Lipomatosis - A Case Report and a Review of the Literature.

Authors:  Dietmar Dammerer; Johannes Neugebauer; David Putzer; Benjamin Henninger
Journal:  In Vivo       Date:  2021 Mar-Apr       Impact factor: 2.155

2.  Multiple intraosseous lipomatosis: a case report.

Authors:  Bhavya Rehani; Robert Wissman
Journal:  Cases J       Date:  2009-05-15
  2 in total

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