Advanced search×

Infantile cortical hyperostosis.

D Suri, D Dayal, and M Singh

Arch Dis Child 90(7):711 (2005) PMID 15970613 PMCID PMC1720499

Version: za2963e q8zab q8zbb q8zc2 q8zd1 q8ze6 q8zfd q8zgf
View PDF

Similar articles you may find interesting…

  1. COL1A1 mutation in an Indian child with Caffey disease.
    Prajnya P Ranganath, Christine M CM Laine, and Shubha R SR Phadke

    Indian J Pediatr 78(7):877-9 (2011) PMID 21249479

    Caffey disease or infantile cortical hyperostosis is a rare skeletal disorder with both sporadic and familial occurrence. The autosomal dominant familial form has been found to be a collagenopathy. The case being reported is a 7- month-old Indian boy with Caffey disease who was found...
  2. [Usefulness of ultrasound in infantile cortical hyperostosis].
    S S Haddad-Zebouni, G G Nawfal, and M M Ghossain

    J Radiol 85(3):338-9 (2004) PMID 15192530