Literature DB >> 6785821

Progressive bony dysplasia in Apert syndrome.

N Beligere, V Harris, S Pruzansky.   

Abstract

Ten patients with Apert syndrome (type I acrocephalosyndactyly) were studied. Seven of these patients were observed from infancy for periods ranging from 2 1/2 to 22 years. The patients presented with limited joint mobility and were found to have multiple radiographic abnormalities, including subluxated or flattened humeral heads, irregularities of the glenoid cavity, and early fusion of the calcaneus to the cuboid bone. The limitation of motion and bony defects were progressive, suggesting that Apert syndrome is a generalized dysplasia.

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Year:  1981        PMID: 6785821     DOI: 10.1148/radiology.139.3.6785821

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


  1 in total

1.  MRI characterization of the glenohumeral joint in Apert syndrome.

Authors:  Tami McHugh; Mary Wyers; Erik King
Journal:  Pediatr Radiol       Date:  2007-04-24
  1 in total

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