Pierre Robin Syndrome: A Case Report

Authors

  • Dr. Santoshi Kankante
  • Dr. Ramesh Kothari
  • Dr. Ganesh Misal
  • Dr. Sunil Natha Mhaske

Keywords:

Cleft palate, Micrognathia, Glossoptosis, Pierre Robin syndrome

Abstract

Pierre Robin syndrome a well-recognized congenital condition characterized by micrognathia, glossoptosis and palatal malformation. Pierre Robin syndrome is also called pierre Sequence because it is caused by sequence of events that happen in the womb, which affects the way the baby develops. We report a case of a one  day neonate who presented with complaints of feeding and respiratory difficulty and was later diagnosed as case of Pierre Robin syndrome. The primary defect lies in the arrested development of mandible leading to a characteristic bird face appearance.

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References

Thakkar NV, Bhatt MJ. Pierre robin syndrome: Rehabilitation of a neonate for nursing with a palatal obturator. J Indian Prosthodont Soc. 2005;5:208-10.

Hsieh Y, Chang C, Tsai H, Yang TC, Lee CC, Tsai Ch. The prenatal diagnosis of pierre-Robin sequence. Prenat Diagn. 1999;19:567-9.

Tanpaiboon P, Kantaputra P, Wejathikul K, Piyamongkol W. c. 595-596 insC of FOXC2underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient. Am J Med Genet A. 2010;152A:737-40.

Robin , P. Backward lowering of the root of the tongue causing respiratory disturbances. Bull Acad Med. 1923;89:38.

Eley RC, Farber S. Hypoplasia of the mandible (micrognathia) as a cause of cyanotic attacks in the newly born infant: report of four cases. Am J Dis Child. 1930;39:1167.

Tomaski SM, Howard GH, Aaal HM. Airway obstruction in the pierre Robin sequence. Laryngoscope. 1995;105:111-4.

Published

2018-06-13

How to Cite

Kankante, D. S., Kothari, D. R., Misal, D. G. . . . . . . . . . . . . . . . ., & Mhaske, D. S. N. . (2018). Pierre Robin Syndrome: A Case Report. VIMS Health Science Journal, 5(2), 80–81. Retrieved from https://vimshsj.edu.in/index.php/main/article/view/232

Issue

Section

Case Report

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