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Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease

  • Published:2016-01-14 Issue:4 Volume:170 Page:978-985
  • ISSN:1552-4825
  • Container-title:American Journal of Medical Genetics Part A
  • language:en
  • Short-container-title:Am. J. Med. Genet.

Author:

Gottesman Gary S.1,Madson Katherine L.1,McAlister William H.2,Nenninger Angela1,Wenkert Deborah1,Mumm Steven13,Whyte Michael P.13

Affiliation:

1. Center for Metabolic Bone Disease and Molecular Research; Shriners Hospital for Children; St. Louis Missouri

2. Mallinckrodt Institute of Radiology; Washington University School of Medicine at St. Louis Children's Hospital; St. Louis Missouri

3. Division of Bone and Mineral Diseases at Barnes-Jewish Hospital; Washington University School of Medicine; St. Louis Missouri

Funder

Shriners Hospitals for Children

Clark and Mildred Cox Inherited Metabolic Bone Disease Research Fund

Hypophosphatasia Research Fund

Foundation for Barnes-Jewish Hospital

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference48 articles.

1. Bilateral cavernous internal carotid aneurysms in a child with juvenile Paget disease and osteoprotegerin deficiency;Allen;AJNR Am J Neuroradiol,2008

2. Aw J Davies R Cook J-L 2011 http://radiology.casereports.net/index.php/rcr/article/view/

3. Fragile bones and macrocranium;Bakwin;J Pediatr,1956

4. Osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification;Bucay;Genes Dev,1998
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