References
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.
Robin P. La Glossoptose, Un grave danger pour Nos enfants. Paris, Gaston Doin, 1929.
Caroll DB, Pererson RA, Worton EW and Birnadaum LM. Heredity factors in Pierre Robin syndrome.Brit J Plast Surg 1971; 24: 43–46.
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.
Smith SL, Cavanaugh JJA and Stowe FC. Ocular manifestations of the Pierre Robinsyndrome.Arch Ophthal 1960; 63: 984–992.
Handbook of congenital malformations. Ed. Rubin A. Saunders Company, Philadelphia & London, 1969; 145–146.
Weseman C. Congenital micrognathia.Arch Otolaryn 1959; 69: 31–34.
Cohen MM Jr. The Robin anomalad, its nonspecificity and associated syndromes.J Oral Surg 1976; 34: 587–591.
Smith DW, Classification, nomenclature and naming of morphologic defects.J Pediatr 1975; 87: 162–164
Meckenzi J. The first arch syndrome.Arch Dis Child 1958; 33: 477–486.
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.
Warkany J. Congenital malformations induced by maternal nutritional deficiency.J Pediatr 1966; 25: 476–479.
Cocke W Jr. Experimental production of micrognathia and glossoptosis associated with cleft palate (Pierre Robin syndrome).Plast and Reconstr Surg 1966; 38: 395–403.
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.
Pfaff HW. Quoted in Burnning and Schwalbe’s“Handbuch der allagemeinen pathologie und der pathologischen Anatomie des kindes alters. Munich 1913; 2: 442
Mckusick VA. ‘MandelianInheritance in Man’. 2nd Ed., Baltimore, John Hapskins Press. 1966; 346
Holthusen W. The Pierre Robin syndrome, unusual associated developmental defects.Ann Radiol 1971; 15: 253–263.
Holdsworth WG.Cleft lip and palate. Heinemann, London. 1963.
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.
Edwards JRG, Newell DR. The Pierre Robin Syndrome reassessed in the light of recent research.Br J Plast Surg 1985; 38: 339–342.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
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
Issue Date:
DOI: https://doi.org/10.1007/BF02722316