Prenatal Sonographic Diagnosis of Pierre-Robin Sequence - A Case Report

• Authors: Rafał Zieliński , Sebastian Foryś , Maria Respondek-Liberska
• Languages of publication: EN

Abstracts

EN

The rare anomalies diagnosed in prenatal ultrasonographic examination include Pierre-Robin sequence. The aim of the report was to demonstrate a well-documented case of Pierre-Robin sequence detected by ultrasonography at the 24th week of gestation, present the differentiation of Pierre-Robin sequence in the prenatal ultrasonography and to emphasize the importance of early sonographic diagnosis of the anomaly.The prenatal diagnosis of Pierre-Robin sequence in prenatal ultrasonographic assessment is of great importance as it permits planning further course of pregnancy as well as EXIT procedure and postnatal treatment.

Keywords

EN

fetus; micrognathia; retrognathia; Pierre-Robin sequence; ultrasonography

• Publisher: De Gruyter Open
• Journal: Prenatal Cardiology
• Year: 2015
• Volume: 5
• Issue: 2
• Pages: 21-23

Dates

published

1 - 6 - 2015

received

18 - 5 - 2015

accepted

28 - 6 - 2015

online

30 - 12 - 2015

Contributors

author

Rafał Zieliński

• Department of Pediatric Laryngology, Medical University of Lodz, Poland

author

Sebastian Foryś

• Department of Radiology, Polish Mother's Memorial Hospital Research Institute, Lodz, Poland

author

Maria Respondek-Liberska

• Department of Prenatal Cardiology, Polish Mother's Memorial Hospital Research Institute, Lodz, Poland
• Department of Diagnoses and Prevention Fetal Malformations Medical University of Lodz, Poland

References

• 1. Zielinski R, Respondek-Liberska M.: Craniofacial malformations in prenatal ultrasound evaluation. Literature review. Ginekol Pol 2013, 9: 801-806
• 2. Shprintzen RJ.: The implications of the diagnosis of Robin sequence. Cleft Palate Craniofac J 1992, 3: 205-209
• 3. Zielinski R, Respondek-Liberska M.: Retrospective chart review of 44 fetuses with cervicofacial tumors in the sonographic assessment. Int J Pediatr Otorhinolaryngol 2015, 3:363-368[Crossref][WoS]
• 4. Chiriac A, Dawson A, Krapp M, Axt-Fliedner R.: Pierre- Robin syndrome: a case report. Arch Gynecol Obstet 2008, 1: 95-98
• 5. Paladini D, Volpe P.: Micrognatia. Ultrasound of Congenital Fetal Anomalies. London 2007, Informa UK Ltd: 93-95
• 6. Kosmaidou-Aravidou Z, Siabalioti G, Karpathios S, Grigori P, Panani A.: Prenatal diagnosis of a cervical teratoma with a cytogenetic study. J Matern Fetal Neonatal Med 2006, 6: 377-379
• 7. Dighe MK, Peterson SE, Dubinsky TJ, Perkins J, Cheng E.: EXIT procedure: technique and indications with prenatal imaging parameters for assessment of airway patency. Radiographics 2011, 2: 511-526[WoS][Crossref]
• 8. Laje P, Johnson MP, Howell LJ, Bebbington MW, Hedrick HL, Flake AW, et al.: Ex utero intrapartum treatment in the management of giant cervical teratomas. J Pediatr Surg 2012, 6: 1208-1216[Crossref]
• 9. Costello BJ, Hueser T, Mandell D, Hackam D, Prosen TL.: Syndromic micrognathia and peri-natal management with the ex-utero intra-partum treatment (EXIT) procedure. Int J Oral Maxillofac Surg 2010, 7: 725-728[WoS]
• 10. Caouette-Laberge L, Borsuk DE, Bortoluzzi PA.: Subperiosteal release of the floor of the mouth to correct airway obstruction in Pierre-Robin sequence: review of 31 cases. Cleft Palate Craniofac J 2012, 1: 14-20[WoS]
• 11. Benacerraf BR.: Micrognathia. Ultrasound of Fetal Syndromes. 2nd ed. Philadelphia 2008, Churchill Livingstone Elseviere; 2008. p. 8-10.

Identifiers

DOI

10.12847/06154