Radiological case of the month

Applied Radiology

Volumn 35, Issue 7, 2006, Pages 38-42

  Beall, Douglas P ^a   Emery, Robert L ^a   Ly, Justin Q ^b   Jones, Thomas P ^c  

^a UNIFORMED SERVICES UNIVERSITY OF THE HEALTH SCIENCES   (United States)

^b WILFORD HALL MEDICAL CENTER   (United States)

^c MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETABULUM; ACHONDROPLASIA; ARTICLE; CASE REPORT; CHILDHOOD DISEASE; CLINICAL FEATURE; ELBOW RADIOGRAPHY; EPIPHYSIS; FEMALE; FEMUR NECK; FOOT RADIOGRAPHY; HUMAN; IMAGE ANALYSIS; METAPHYSIS; PHYSICAL EXAMINATION; PSEUDOACHONDROPLASIA; SCHOOL CHILD; SHORT STATURE;

EID: 33748745131     PISSN: 01609963     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Kornblum M, Stanitski DF. Spinal manifestations of skeletal dysplasia. Orthop Clin North Am. 1999;30:501-520.
2. Wynne-Davies R, Hall CM, Apley AG. Atlas of Skeletal Dysplasias. New York, NY: Churchill Livingstone; 1985:239-242.
3. Hecht JT, Montufar-Solis D, Decker G, et al. Retention of cartilage oligomeric matrix protein (COMP) and cell death in redifferentiated pseudoachondroplasia chondrocytes. Matrix Biol. 1998; 17: 625-633.
4. Holden P, Meadows RS, Chapman KL, et al. Cartilage oligomeric matrix protein interacts with type IX collagen, and disruptions to these interactions identify a pathogenetic mechanism in a bone dysplasia family. J Biol Chem. 2001;276:6046-6055.
5. Briggs MD, Hoffman SM, King LM, et al. Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene. Nat Genet. 1995;10:330-336.
6. McKeand J, Rotta J, Hecht JT. Natural history of pseudoachondroplasia. Am J Med Genet. 1996;63:406-410.