Bruck syndrome: A rare combination of bone fragility and multiple congenital joint contractures

Journal of Pediatric Orthopaedics Part B

Volumn 7, Issue 1, 1998, Pages 35-38

  Breslau Siderius, E J ^a   Engelbert, R H B ^b   Pals, G ^c   Van Der Sluijs, J A ^b  

^a Clinical Genetics Center Utrecht   (Netherlands)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c VU UNIVERSITY AMSTERDAM   (Netherlands)

Author keywords

Arthogryposis congenita; Bruck syndrome; Osteogenesis imperfecta

Indexed keywords

ARTHROGRYPOSIS; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BONE RADIOGRAPHY; CASE REPORT; CHILD; FEMALE; HUMAN; JOINT CONTRACTURE; MALE; OSTEOGENESIS IMPERFECTA; OSTEOPOROSIS; PRIORITY JOURNAL; SCOLIOSIS;

EID: 0031930903     PISSN: 1060152X     EISSN: None     Source Type: Journal    
DOI: 10.1097/01202412-199801000-00006     Document Type: Article

References (4)

1. Brenner RE, Vetter U, Stoss H, Muller PK, Teller WM. Defective collagen fibril formation and mineralisation in osteogenesis imperfecta with congenital joint contractures (Bruck syndrome). Eur J Pediatr 1993;152:505-8.
2. Bruck A. Ueber eine seltene form von Erkrankung der Knochen und Gelenke. Dtsch Med Wochenschr 1897;23:152-5.
3. Sharma NL, Anand JS. Osteogenesis imperfecta with arthrogryposis multiplex congenita. J Indian Med Assoc 1964;43:124-6.
4. Viljoen D, Versfeld G, Beighton P. Osteogenesis imperfecta with congenital joint contractures (Bruck syndrome). Clin Genet 1989; 36:122-6.