Skip to main content
PMC home page
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1988 Aug;25(8):557–560. doi: 10.1136/jmg.25.8.557

Russell-Silver syndrome.

M A Patton 1
PMCID: PMC1080034  PMID: 3050100

Full text

PDF
559

Images in this article

557Image
on p.557
558Image
on p.558
558Image
on p.558

Selected References

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

  1. Abramowicz H. K., Nitowsky H. M. Reproductive ability of an adult female with Silver-Russell syndrome. J Med Genet. 1977 Apr;14(2):134–136. doi: 10.1136/jmg.14.2.134. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Angehrn V., Zachmann M., Prader A. Silver-Russell syndrome. Observations in 20 patients. Helv Paediatr Acta. 1979 Sep;34(4):297–308. [PubMed] [Google Scholar]
  3. BLACK J. Low birth weight dwarfism. Arch Dis Child. 1961 Dec;36:633–644. doi: 10.1136/adc.36.190.633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chauvel P. J., Moore C. M., Haslam R. H. Trisomy-18 mosaicism with features of Russel-Silver syndrome. Dev Med Child Neurol. 1975 Apr;17(2):220–224. doi: 10.1111/j.1469-8749.1975.tb03473.x. [DOI] [PubMed] [Google Scholar]
  5. Escobar V., Gleiser S., Weaver D. D. Phenotypic and genetic analysis of the silver-Russell syndrome. Clin Genet. 1978 Mar;13(3):278–288. doi: 10.1111/j.1399-0004.1978.tb01182.x. [DOI] [PubMed] [Google Scholar]
  6. FERRIER P., STALDER G., BAMATTER F., FERRIER S., BUEHLER E., KLEIN D. CONGENITAL ASYMMETRY ASSOCIATED WITH DIPLOID-TRIPLOID MOSAICISM AND LARGE SATELLITES. Lancet. 1964 Jan 11;1(7324):80–82. doi: 10.1016/s0140-6736(64)91395-9. [DOI] [PubMed] [Google Scholar]
  7. Fitch N., Pinsky L. The lateral facial profile of the Silver-Russell dwarf. J Pediatr. 1972 May;80(5):827–829. doi: 10.1016/s0022-3476(72)80138-0. [DOI] [PubMed] [Google Scholar]
  8. Haslam R. H., Berman W., Heller R. M. Renal abnormalities in the Russell-Silver syndrome. Pediatrics. 1973 Feb;51(2):216–222. [PubMed] [Google Scholar]
  9. Keppen L. D., Rennert O. M. Silver-Russell syndrome with absence of digits and syndactylism of the fingers. Clin Genet. 1983 Dec;24(6):453–455. doi: 10.1111/j.1399-0004.1983.tb00103.x. [DOI] [PubMed] [Google Scholar]
  10. Marks L. J., Bergeson P. S. The Silver-Russel syndrome: a case with sexual ambiguity, and a review of literature. Am J Dis Child. 1977 Apr;131(4):447–451. doi: 10.1001/archpedi.1977.02120170073015. [DOI] [PubMed] [Google Scholar]
  11. Partington M. W. X-linked short stature with skin pigmentation: evidence for heterogeneity of the Russell-Silver syndrome. Clin Genet. 1986 Feb;29(2):151–156. doi: 10.1111/j.1399-0004.1986.tb01240.x. [DOI] [PubMed] [Google Scholar]
  12. SILVER H. K., KIYASU W., GEORGE J., DEAMER W. C. Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins. Pediatrics. 1953 Oct;12(4):368–376. [PubMed] [Google Scholar]
  13. SZALAY G. C. PSEUDOHYDROCEPHALUS IN DWARFS. THE RUSSELL DWARF. J Pediatr. 1963 Oct;63:622–633. doi: 10.1016/s0022-3476(63)80372-8. [DOI] [PubMed] [Google Scholar]
  14. Saal H. M., Pagon R. A., Pepin M. G. Reevaluation of Russell-Silver syndrome. J Pediatr. 1985 Nov;107(5):733–737. doi: 10.1016/s0022-3476(85)80402-9. [DOI] [PubMed] [Google Scholar]
  15. Snow R., Sacks M. O., Cornblath M. Ketotic hypoglycemia in a Russell dwarf. J Pediatr. 1966 Jul;69(1):121–125. doi: 10.1016/s0022-3476(66)80369-4. [DOI] [PubMed] [Google Scholar]
  16. Tanner J. M., Lejarraga H., Cameron N. The natural history of the Silver-Russell syndrome: a longitudinal study of thirty-nine cases. Pediatr Res. 1975 Aug;9(8):611–623. doi: 10.1203/00006450-197508000-00001. [DOI] [PubMed] [Google Scholar]
  17. Tulinius H., Tryggvason K., Hauksdottir H. 45, X-46, XY chromosome mosaic with features of the Russell-Silver syndrome: a case report with a review of the literature. Dev Med Child Neurol. 1972 Apr;14(2):161–172. doi: 10.1111/j.1469-8749.1972.tb02574.x. [DOI] [PubMed] [Google Scholar]
  18. Wiedemann H. R. An unidentified neonatal progeroid syndrome: follow-up report. Eur J Pediatr. 1979 Jan 18;130(1):65–70. doi: 10.1007/BF00441901. [DOI] [PubMed] [Google Scholar]
  19. Winter R. M., Baraitser M., Grant D. B., Preece M. A., Hall C. M. The 3-M syndrome. J Med Genet. 1984 Apr;21(2):124–128. doi: 10.1136/jmg.21.2.124. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES