Skip to main content
Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1969 Aug;44(236):490–498. doi: 10.1136/adc.44.236.490

Dysplasia spondyloepiphysaria congenita and related generalized skeletal dysplasias among children with severe visual handicaps.

G R Fraser, A I Friedmann, P Maroteaux, A M Glen-Bott, U Mittwoch
PMCID: PMC2020135  PMID: 5803642

Full text

PDF
490

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BRAUN O. H., MEYTHALER H. [Endochondral dysostosis (Bartenwerfer type)]. Arch Kinderheilkd. 1962 Mar;166:89–96. [PubMed] [Google Scholar]
  2. CIGALA F., GOLINO M. CONSIDERAZIONI PATOGENETICHE SU UN CASO DI MORBO DI MORQUIO-ULLRICH. Pediatria (Napoli) 1964 Aug 31;72:800–809. [PubMed] [Google Scholar]
  3. DAVID B. Uber einen dominanten Erbgang bei einer polytopen enchondralen Dysostose Typ Pfaundler-Hurler. Z Orthop Ihre Grenzgeb. 1954;84(4):657–660. [PubMed] [Google Scholar]
  4. FRASER F. C., SCRIVER J. B. A hereditary factor in chondrodystrophia calcificans congenita. N Engl J Med. 1954 Feb 18;250(7):272–277. doi: 10.1056/NEJM195402182500702. [DOI] [PubMed] [Google Scholar]
  5. HATT J. J. Polydystrophie de Hürler chez un prématuré; association d'une cataracte congenitale. Strasb Med. 1952 Dec;3(12):893–896. [PubMed] [Google Scholar]
  6. KNIEST W. Zur Abgrenzung der Dysostosis enchondralis von der Chondrodystrophie. Z Kinderheilkd. 1952;70(6):633–640. [PubMed] [Google Scholar]
  7. LAMY M., MAROTEAUX P. [Diastrophic nanism]. Presse Med. 1960 Nov 23;68:1977–1980. [PubMed] [Google Scholar]
  8. MANTOVANI V., NORDIO S. Le sindromi di Ehlers-Danlos e di Brailsford-Morquio; loro rapporti nosologici. Minerva Pediatr. 1956 Oct 27;8(43):1316–1331. [PubMed] [Google Scholar]
  9. MAROTEAUX P., LAMY M., BERNARD J. La dysplasie spondylo-epiphysaire tardive; description clinique et radiologique. Presse Med. 1957 Jun 26;65(51):1205–1208. [PubMed] [Google Scholar]
  10. MOORE W. T., FEDERMAN D. D. FAMILIAL DWARFISM AND "STIFF JOINTS". Arch Intern Med. 1965 Apr;115:398–404. doi: 10.1001/archinte.1965.03860160024004. [DOI] [PubMed] [Google Scholar]
  11. Maroteaux P., Spranger J., Wiedemann H. R. Der metatropische Zwergwuchs. Arch Kinderheilkd. 1966 Feb;173(3):211–226. [PubMed] [Google Scholar]
  12. ROSENBLOOM A. L., SMITH D. W. THE NATURAL HISTORY OF METAPHYSEAL DYSOSTOSIS. J Pediatr. 1965 May;66:857–868. doi: 10.1016/s0022-3476(65)80060-9. [DOI] [PubMed] [Google Scholar]
  13. Roaf R., Longmore J. B., Forrester R. M. A childhood syndrome of bone dysplasia, retinal detachment and deafness. Dev Med Child Neurol. 1967 Aug;9(4):464–473. doi: 10.1111/j.1469-8749.1967.tb02300.x. [DOI] [PubMed] [Google Scholar]
  14. SCHEIE H. G., HAMBRICK G. W., Jr, BARNESS L. A. A newly recognized forme fruste of Hurler's disease (gargoylism). Am J Ophthalmol. 1962 May;53:753–769. [PubMed] [Google Scholar]
  15. STICKLER G. B., BELAU P. G., FARRELL F. J., JONES J. D., PUGH D. G., STEINBERG A. G., WARD L. E. HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY. Mayo Clin Proc. 1965 Jun;40:433–455. [PubMed] [Google Scholar]
  16. UHLIG H. Dysostosis enchondralis, Typ Bartenwerfer. Arch Kinderheilkd. 1954;148(1):22–31. [PubMed] [Google Scholar]
  17. VON NOORDEN G. K., ZELLWEGER H., PONSETI I. V. Ocular findings in Morquio-Ullrich's disease. With report of two cases. Arch Ophthalmol. 1960 Oct;64:585–591. doi: 10.1001/archopht.1960.01840010587017. [DOI] [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood are provided here courtesy of BMJ Publishing Group

RESOURCES