The Indian Journal of Pediatrics

, Volume 56, Issue 3, pp 413–417 | Cite as

Pierre Robin syndrome : Autosomal dominant inheritance with pleiotropic effect

  • S. S. Sidhu
  • R. N. Deshmukh
Clinical Briefs: Cutaneous Erythropoiesis


Club Foot Cleft Palate Synostosis Pyloric Stenosis Stickler Syndrome 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


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  1. 1.
    Robin P. La chute de la is base de la tongue consideree commeune nouvelle cause de gene dans is respiration nasopharyngienne.Bulletin de Academic Nationale de Me’decine, 1923; 89: 37–40.Google Scholar
  2. 2.
    Robin P. La Glossoptose, Un grave danger pour Nos enfants. Paris, Gaston Doin, 1929.Google Scholar
  3. 3.
    Caroll DB, Pererson RA, Worton EW and Birnadaum LM. Heredity factors in Pierre Robin syndrome.Brit J Plast Surg 1971; 24: 43–46.CrossRefGoogle Scholar
  4. 4.
    Shah CV, Pruzansky S, Harris WS. Cardiac malformations with facial clefts, with observations on the Pierre Robin syndrome.Am J Dis Child 1970; 119: 238–444.PubMedGoogle Scholar
  5. 5.
    Smith SL, Cavanaugh JJA and Stowe FC. Ocular manifestations of the Pierre Robinsyndrome.Arch Ophthal 1960; 63: 984–992.PubMedGoogle Scholar
  6. 6.
    Handbook of congenital malformations. Ed. Rubin A. Saunders Company, Philadelphia & London, 1969; 145–146.Google Scholar
  7. 7.
    Weseman C. Congenital micrognathia.Arch Otolaryn 1959; 69: 31–34.Google Scholar
  8. 8.
    Cohen MM Jr. The Robin anomalad, its nonspecificity and associated syndromes.J Oral Surg 1976; 34: 587–591.PubMedGoogle Scholar
  9. 9.
    Smith DW, Classification, nomenclature and naming of morphologic defects.J Pediatr 1975; 87: 162–164PubMedCrossRefGoogle Scholar
  10. 10.
    Meckenzi J. The first arch syndrome.Arch Dis Child 1958; 33: 477–486.CrossRefGoogle Scholar
  11. 11.
    Smith JL and Stowe FC. The Pierre Robin syndrome (glossoptosis, micrognathia, cleft palate): A review of thirty nine cases with emphasis on associated ocular lesions.Pediatrics 1961; 27 : 128–133.Google Scholar
  12. 12.
    Warkany J. Congenital malformations induced by maternal nutritional deficiency.J Pediatr 1966; 25: 476–479.Google Scholar
  13. 13.
    Cocke W Jr. Experimental production of micrognathia and glossoptosis associated with cleft palate (Pierre Robin syndrome).Plast and Reconstr Surg 1966; 38: 395–403.CrossRefGoogle Scholar
  14. 14.
    Latham RA. The pathogenesis of cleft palate associated with the PR syndrome : An analysis of a seventeen week human fetus.Brit J Plast Surg 1966; 205–214.Google Scholar
  15. 15.
    Pfaff HW. Quoted in Burnning and Schwalbe’s“Handbuch der allagemeinen pathologie und der pathologischen Anatomie des kindes alters. Munich 1913; 2: 442Google Scholar
  16. 16.
    Mckusick VA. ‘MandelianInheritance in Man’. 2nd Ed., Baltimore, John Hapskins Press. 1966; 346Google Scholar
  17. 17.
    Holthusen W. The Pierre Robin syndrome, unusual associated developmental defects.Ann Radiol 1971; 15: 253–263.Google Scholar
  18. 18.
    Holdsworth WG.Cleft lip and palate. Heinemann, London. 1963.Google Scholar
  19. 19.
    Rintala A, Ranta R, Stegars T. On pathogenesis of cleft palate in the Pierre Robin syndrome.Scand J Plast Reconstr Surg 1984; 18: 237–240.PubMedGoogle Scholar
  20. 20.
    Edwards JRG, Newell DR. The Pierre Robin Syndrome reassessed in the light of recent research.Br J Plast Surg 1985; 38: 339–342.PubMedCrossRefGoogle Scholar

Copyright information

© Dr. K C Chaudhuri Foundation 1989

Authors and Affiliations

  • S. S. Sidhu
    • 1
  • R. N. Deshmukh
    • 1
  1. 1.Department of Dental SurgeryAll India Institute of Medical SciencesNew Delhi

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