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Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1990 Aug;27(8):512–515. doi: 10.1136/jmg.27.8.512

Dyggve-Melchior-Clausen syndrome.

P Beighton 1
PMCID: PMC1017201  PMID: 2213845

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Selected References

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

  1. Beck M., Lücke R., Kresse H. Dyggve-Melchior-Clausen syndrome: normal degradation of proteodermatan sulfate, proteokeratan sulfate and heparan sulfate. Clin Chim Acta. 1984 Aug 15;141(1):7–15. doi: 10.1016/0009-8981(84)90161-x. [DOI] [PubMed] [Google Scholar]
  2. Beemer F. A., Hennekam R. C. Het Dyggve-Melchior-Clausen syndroom. Tijdschr Kindergeneeskd. 1984 Jun;52(3):103–107. [PubMed] [Google Scholar]
  3. Bonafede R. P., Beighton P. The Dyggve-Melchior-Clausen syndrome in adult siblings. Clin Genet. 1978 Jul;14(1):24–30. doi: 10.1111/j.1399-0004.1978.tb02056.x. [DOI] [PubMed] [Google Scholar]
  4. Bonafede R. P., Beighton P. The Dyggve-Melchior-Clausen syndrome in adult siblings. Clin Genet. 1978 Jul;14(1):24–30. doi: 10.1111/j.1399-0004.1978.tb02056.x. [DOI] [PubMed] [Google Scholar]
  5. Hall-Craggs M. A., Chapman M. Case report 431: Dyggve-Melchior-Clausen syndrome (DMCS). Skeletal Radiol. 1987;16(5):422–424. doi: 10.1007/BF00350972. [DOI] [PubMed] [Google Scholar]
  6. Naffah J., Taleb N. Deux nouveaux cas de syndrome de Dyggve Melchior Clausen avec hypoplasie de l'apophyse odontoide et compression spinale. Arch Fr Pediatr. 1974 Dec;31(10):985–992. [PubMed] [Google Scholar]
  7. Naffah J. The Dyggve-Melchior-Clausen syndrome. Am J Hum Genet. 1976 Nov;28(6):607–614. [PMC free article] [PubMed] [Google Scholar]
  8. Rastogi S. C., Clausen J., Melchior J. C., Dyggve H. V. Abnormal serum alpha 2-macroglobulin in Dyggve-Melchior-Clausen syndrome. J Clin Chem Clin Biochem. 1980 Jan;18(1):67–68. [PubMed] [Google Scholar]
  9. Rastogi S. C., Clausen J., Melchior J. C., Dyggve H. V., Jensen G. E. Lysosomal (leucocyte) proteinase and sulfatase levels in Dyggve-Melchior-Clausen (DMC) syndrome. Acta Neurol Scand. 1977 Nov;56(5):389–396. doi: 10.1111/j.1600-0404.1977.tb01446.x. [DOI] [PubMed] [Google Scholar]
  10. SMITH R., McCORT J. J. Osteochondrodystrophy (Morquio-Brailsford type); occurrence in three siblings. Calif Med. 1958 Jan;88(1):55–59. [PMC free article] [PubMed] [Google Scholar]
  11. Spranger J., Bierbaum B., Herrmann J. Heterogeneity of Dyggve-Melchior-Clausen dwarfism. Hum Genet. 1976 Aug 30;33(3):279–287. doi: 10.1007/BF00286853. [DOI] [PubMed] [Google Scholar]
  12. Spranger J., Maroteaux P., Der Kaloustian V. M. The Dyggve-Melchior-Clausen syndrome. Radiology. 1975 Feb;114(2):415–421. doi: 10.1148/114.2.415. [DOI] [PubMed] [Google Scholar]
  13. Toledo S. P., Saldanha P. H., Lamego C., Mourão P. A., Dietrich C. P., Mattar E. Dyggve-Melchior-Clausen syndrome: genetic studies and report of affected sibs. Am J Med Genet. 1979;4(3):255–261. doi: 10.1002/ajmg.1320040308. [DOI] [PubMed] [Google Scholar]

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