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Pierre Robin syndrome : Autosomal dominant inheritance with pleiotropic effect

  • Clinical Briefs: Cutaneous Erythropoiesis
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References

  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. Robin P. La Glossoptose, Un grave danger pour Nos enfants. Paris, Gaston Doin, 1929.

    Google Scholar 

  3. Caroll DB, Pererson RA, Worton EW and Birnadaum LM. Heredity factors in Pierre Robin syndrome.Brit J Plast Surg 1971; 24: 43–46.

    Article  Google Scholar 

  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.

    PubMed  CAS  Google Scholar 

  5. Smith SL, Cavanaugh JJA and Stowe FC. Ocular manifestations of the Pierre Robinsyndrome.Arch Ophthal 1960; 63: 984–992.

    PubMed  CAS  Google Scholar 

  6. Handbook of congenital malformations. Ed. Rubin A. Saunders Company, Philadelphia & London, 1969; 145–146.

    Google Scholar 

  7. Weseman C. Congenital micrognathia.Arch Otolaryn 1959; 69: 31–34.

    CAS  Google Scholar 

  8. Cohen MM Jr. The Robin anomalad, its nonspecificity and associated syndromes.J Oral Surg 1976; 34: 587–591.

    PubMed  Google Scholar 

  9. Smith DW, Classification, nomenclature and naming of morphologic defects.J Pediatr 1975; 87: 162–164

    Article  PubMed  CAS  Google Scholar 

  10. Meckenzi J. The first arch syndrome.Arch Dis Child 1958; 33: 477–486.

    Article  Google Scholar 

  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. Warkany J. Congenital malformations induced by maternal nutritional deficiency.J Pediatr 1966; 25: 476–479.

    Google Scholar 

  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.

    Article  Google Scholar 

  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.

  15. Pfaff HW. Quoted in Burnning and Schwalbe’s“Handbuch der allagemeinen pathologie und der pathologischen Anatomie des kindes alters. Munich 1913; 2: 442

    Google Scholar 

  16. Mckusick VA. ‘MandelianInheritance in Man’. 2nd Ed., Baltimore, John Hapskins Press. 1966; 346

    Google Scholar 

  17. Holthusen W. The Pierre Robin syndrome, unusual associated developmental defects.Ann Radiol 1971; 15: 253–263.

    Google Scholar 

  18. Holdsworth WG.Cleft lip and palate. Heinemann, London. 1963.

    Google Scholar 

  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.

    PubMed  CAS  Google Scholar 

  20. Edwards JRG, Newell DR. The Pierre Robin Syndrome reassessed in the light of recent research.Br J Plast Surg 1985; 38: 339–342.

    Article  PubMed  CAS  Google Scholar 

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Sidhu, S.S., Deshmukh, R.N. Pierre Robin syndrome : Autosomal dominant inheritance with pleiotropic effect. Indian J Pediatr 56, 413–417 (1989). https://doi.org/10.1007/BF02722316

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