Pierre Robin sequence with esophageal atresia and congenital radioulnar synostosis

Cleft Palate-Craniofacial Journal

Volumn 43, Issue 3, 2006, Pages 317-320

  Ozkan, Keramettin Ugur ^a   Coban, Yusuf Kenan ^a   Uzel, Murat ^a   Ergun, Mehmet ^b   Oksuz, Hafize ^a  

^a KAHRAMANMARAS SUTCU IMAM UNIVERSITY   (Turkey)

^b GAZI UNIVERSITY FACULTY OF MEDICINE   (Turkey)

Author keywords

Congenital radioulnar synostosis; Esophageal atresia; Pierre Robin sequence

Indexed keywords

ARTICLE; CASE REPORT; CLEFT PALATE; ESOPHAGUS ATRESIA; GLOSSOPTOSIS; HUMAN; JAW MALFORMATION; LOW SET EAR; MALE; MICROGNATHA; MICROTIA; NEWBORN; PIERRE ROBIN SYNDROME; PRIORITY JOURNAL; RADIOULNAR SYNOSTOSIS; SYNOSTOSIS; TONGUE DISEASE;

ESOPHAGEAL ATRESIA; HUMANS; INFANT, NEWBORN; MALE; PIERRE ROBIN SYNDROME; RADIUS; SYNOSTOSIS; TRACHEOESOPHAGEAL FISTULA; ULNA;

EID: 33646872434     PISSN: 10556656     EISSN: None     Source Type: Journal    
DOI: 10.1597/05-032R1.1     Document Type: Article

References (30)

1. Arya SK, Chaudhuri Z, Jain R, Nahar R, Sood S. Congenital alacrima in Pierre Robin Sequence. Cornea. 2004;23:632-634.
2. Azmy AF, Raine PA, Young DG. Orofacial clefts and esophageal atresia. Arch Dis Child. 1983;58:639-641.
3. Benson JE, Olsen MM, Fletcher BD. A spectrum of bronchopulmonary anomalies associated with tracheoesophageal malformations. Pediatr Radiol. 1985;15:377-380.
4. Cano Garci-Nuno A, Solis Sanchez G, Coto Cotallo GD, Cepeda Martinez A, Ramos Aparicio A, Lopez Sastre J, Crespo Hernandez M. Esophageal atresia and associated anomalies. An Esp Pediatr. 1992;36:455-459.
5. Cohen MM Jr. Interface between Robin sequence and ordinary cleft palate. Am J Med Genet. 2001;101:288.
6. Doray B, Langer B, Stoll C. Two cases of Townes-Brocks syndrome. Genet Couns. 1999;10:359-367.
7. Ein SH, Shandling B, Wesson D, Filler RM. Esophageal atresia with distal tracheoesophageal fistula: associated anomalies and prognosis in the 1980s. J Pediatr Surg. 1989;24:1055-1059.
8. Fernbach SK, Glass RBJ. The expanded spectrum of limb anomalies in the VATER association. Pediat Radiol. 1988;18:215-220.
9. Giuffre L, Corsello G, Giuffre M, Piccione M, Albanese A. A new syndrome: autosomal dominant microcephaly and radioulnar synostosis. Am J Med Genet. 1994;51:266-269.
10. Gurrieri F, Scarano G, Garavelli L, Della Monica M, Lonardo F, Cuda D, Banchini G, Opitz JM, Neri G. Mental retardation, Robin sequence and brachydactyly. Further confirmation of a new syndrome. Am J Med Genet A. 2004; 126:204-207.
11. Guvener M, Demircin M. Giant aneurysm of the ductus arteriosus in an infant with Pierre-Robin sequence. Pediatr Cardiol. 2003;24:309-320.
12. Hanson JW, Smith DW. U-shaped palatal defect in the Robin anomalad: developmental and clinical relevance. J Pediatr. 1975;87:30-33.
13. Holder TM, Cloud DT, Lewis JE Jr, Pilling GP IV. Esophageal atresia and tracheoesophageal fistula: a survey of its members by the surgical section of the American Academy of Pediatrics. Pediatrics. 1964;34:542-549.
14. Holder-Espinasse M, Abadie V, Cormier-Daire V, Beyler C, Manach Y, Munnich A, Lyonnet S, Couly G, Amiel J. Pierre Robin sequence: a series of 117 consecutive cases. J Pediatr. 2001;139:588-590.
15. Howardy-Hansen P, Berthelsen P. Fiber-optic bronchoscopic nasotracheal intubation of a neonate with Pierre Robin syndrome. Anesthesia. 1988;48:121-122.
16. Kariya S, Nishizaki K, Akagi H, Paparella MM. Abnormal direction of internal auditory canal and vestibulocochlear nerve. J Laryngol Otol. 2004;118:902-905.
17. Lyonnet S, Couly G, Amiel Y. Pierre Robin Sequence: a series of 117 consecutive cases. J Pediatr. 2001;139:588-590.
18. Marques IL, Barbieri MA, Bettiol H. Etiopathogenesis of isolated Robin sequence. Cleft Palate Craniofac J. 1998;35:517-525.
19. Melkoniemi M, Koillinen H, Mannikko M, Warman ML, Pihlajamaa T, Kaariainen H, Rautio J, Hukki J, Stofko JA, Cisneros GJ, Krakow D, Cohn DH, Kere J, Ala-Kokko L. Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence, and micrognathia. Eur J Hum Genet. 2003;11: 265-270.
20. Parent P, Bensaid M, Le Guern H, Colin A, Broussine L, Chabarot A, Cozic A, Jehannin B, de Parscau L. Clinical heterogeneity of Townes-Brocks syndrome [in French]. Arch Pediatr. 1995;2:551-554.
21. Printzlau A, Anderson M. Pierre Robin sequence in Denmark: A Retrospective population-based epidemiological study. Cleft Palate Craniofac J. 2004;41: 47-52.
22. Robin P. Glossoptosis due to atresia and hypotrophy of the mandible. Am J Dis Child. 1934;48:541-547.
23. Robinson GC, Miller JR, Dill FJ, Kamburoff TD. Klinefelter syndrome with the XXYY sex chromosome complex with particular reference to prepubertal diagnosis. J Pediatr. 1964;65:266-232.
24. Rogers NK, Strachan M. Pierre Robin anomalad maculopathy and autolytic cataract. J Pediatr Opthalmos Strabismus. 1995;32:391-392.
25. Seefelder C, Elango S, Rosbe KW, Jennings RW. Oesophageal perforation presenting as oesophageal atresia in a premature neonate following difficult intubation. Paediatr Anaesth. 2001;11:112-118.
26. Shamberger RC, Welch KS. Surgical repair of pectus excavatum. J Pediatr Surg. 1988;23:615-622.
27. Spitz L, Yang X, Pierro A, Kiely M, Drake D. Adverse association of esophageal atresia and cleft lip and palate. Br J Surg. 2003;90:716-717.
28. Tubbs RS, Oakes WS. Pierre Robin syndrome associated with Chiari malformation. Child News Syst. 2004;20:1-2.
29. Verma RS, Babu A. Tissue culture techniques and chromosome preparation. In: Verma RS, Babu A, eds. Human Chromosomes Principles and Techniques. 2nd ed. New York: McGraw-Hill; 1995:6-71.
30. Wang R, Martinez-Frias ML, Graham JM Jr. Infants of diabetic mothers are at increased risk for the oculo-auriculo-vertebral sequence: a case-based and case-control approach. J Pediatr. 2002;141:611-617.